Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv7095770

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:23,191

Description:NC_000001.10:g.(?_19545797)_(19568987_?)del 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: 102 SVs from 30 studies. See in: genome view

Remapped(Score: Perfect):19,219,303-19,242,493

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv7095770	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	19,219,303	19,242,493
nsv7095770	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	19,545,797	19,568,987

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv18786638	deletion	Multiple	Multiple	not provided	Uncertain significance	ClinVar	RCV003119482.2, VCV002426044.2

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18786638	Remapped	Perfect	NC_000001.11:g.(?_ 19219303)_(1924249 3_?)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	19,219,303	19,242,493
nssv18786638	Submitted genomic		NC_000001.10:g.(?_ 19545797)_(1956898 7_?)del	GRCh37 (hg19)		NC_000001.10	Chr1	19,545,797	19,568,987

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
nssv18786638	GRCh37: NC_000001.10:g.(?_19545797)_(19568987_?)del	deletion	germline	not provided	Uncertain significance	ClinVar	RCV003119482.2, VCV002426044.2

No genotype data were submitted for this variant

You are here: NCBI