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dbVar

Database of genomic structural variation

nsv7096736

Organism: Homo sapiens

Study:nstd102 (Clinical Structural Variants)
Variant Type:copy number variation
Method Type:Multiple
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: Yes
Region Size:108

Description:NC_000004.11:g.(?_5576402)_(5576509_?)del AND multiple conditions

Links to Other Resources

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 129 SVs from 29 studies. See in: genome view

Remapped(Score: Perfect):5,574,675-5,574,782

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv7096736	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	5,574,675	5,574,782
nsv7096736	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	5,576,402	5,576,509

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv18790018	deletion	Multiple	Multiple	Acrofacial dysostosis, Weyers type; Chondroectodermal dysplasia; Curry-Hall syndrome; ELLIS-VAN CREVELD SYNDROME; EVC; Ellis Van Creveld syndrome; See individual phenotypes in OMIM allelic variants; WEYERS ACROFACIAL DYSOSTOSIS; WAD	Pathogenic	ClinVar	RCV003113673.1, VCV002427344.2

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18790018	Remapped	Perfect	NC_000004.12:g.(?_ 5574675)_(5574782_ ?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	5,574,675	5,574,782
nssv18790018	Submitted genomic		NC_000004.11:g.(?_ 5576402)_(5576509_ ?)del	GRCh37 (hg19)		NC_000004.11	Chr4	5,576,402	5,576,509

No validation data were submitted for this variant

Clinical Assertions

Variant Call ID	HGVS	Type	Allele Origin	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv18790018	GRCh37: NC_000004.11:g.(?_5576402)_(5576509_?)del	deletion	germline	Acrofacial dysostosis, Weyers type; Chondroectodermal dysplasia; Curry-Hall syndrome; ELLIS-VAN CREVELD SYNDROME; EVC; Ellis Van Creveld syndrome; See individual phenotypes in OMIM allelic variants; WEYERS ACROFACIAL DYSOSTOSIS; WAD	Pathogenic	ClinVar	RCV003113673.1, VCV002427344.2

No genotype data were submitted for this variant

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