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

dbVar

Database of genomic structural variation

nsv4681573

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:66,819

Description:NC_000009.12:g.(?_77209413)_(77276231_?)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: 183 SVs from 41 studies. See in: genome view

Remapped(Score: Perfect):77,209,413-77,276,231

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4681573	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000009.12	Chr9	77,209,413	77,276,231
nsv4681573	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000009.11	Chr9	79,824,329	79,891,147

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv16213311	deletion	Multiple	Multiple	not provided	Pathogenic	ClinVar	RCV001031470.5, VCV000830870.5

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv16213311	Remapped	Perfect	NC_000009.12:g.(?_ 77209413)_(7727623 1_?)del	GRCh38.p12	First Pass	NC_000009.12	Chr9	77,209,413	77,276,231
nssv16213311	Submitted genomic		NC_000009.11:g.(?_ 79824329)_(7989114 7_?)del	GRCh37 (hg19)		NC_000009.11	Chr9	79,824,329	79,891,147

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
nssv16213311	GRCh37: NC_000009.11:g.(?_79824329)_(79891147_?)del	deletion	germline	not provided	Pathogenic	ClinVar	RCV001031470.5, VCV000830870.5

No genotype data were submitted for this variant

You are here: NCBI