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dbVar

Database of genomic structural variation

nsv6309488

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:1,476,712

Description:NC_000012.11:g.(?_88442961)_(89919672_?)dup AND not provided

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: 2768 SVs from 86 studies. See in: genome view

Remapped(Score: Perfect):88,049,184-89,525,895

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6309488	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000012.12	Chr12	88,049,184	89,525,895
nsv6309488	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000012.11	Chr12	88,442,961	89,919,672

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv17973971	duplication	Multiple	Multiple	not provided	Uncertain significance	ClinVar	RCV002048337.3, VCV001514734.3

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv17973971	Remapped	Perfect	NC_000012.12:g.(?_ 88049184)_(8952589 5_?)dup	GRCh38.p12	First Pass	NC_000012.12	Chr12	88,049,184	89,525,895
nssv17973971	Submitted genomic		NC_000012.11:g.(?_ 88442961)_(8991967 2_?)dup	GRCh37 (hg19)		NC_000012.11	Chr12	88,442,961	89,919,672

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
nssv17973971	GRCh37: NC_000012.11:g.(?_88442961)_(89919672_?)dup	duplication	germline	not provided	Uncertain significance	ClinVar	RCV002048337.3, VCV001514734.3

No genotype data were submitted for this variant

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