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

dbVar

Database of genomic structural variation

nsv4450422

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:371,308

Description:GRCh37/hg19 2p13.3-13.2(chr2:71164124-71535431)x3 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: 1099 SVs from 80 studies. See in: genome view

Remapped(Score: Perfect):70,936,994-71,308,301

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4450422	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	70,936,994	71,308,301
nsv4450422	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000002.11	Chr2	71,164,124	71,535,431

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv15774938	copy number gain	Multiple	Multiple	not provided	Uncertain significance	ClinVar	RCV000846600.2, VCV000685892.2	3

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15774938	Remapped	Perfect	NC_000002.12:g.(?_ 70936994)_(7130830 1_?)dup	GRCh38.p12	First Pass	NC_000002.12	Chr2	70,936,994	71,308,301
nssv15774938	Submitted genomic		NC_000002.11:g.(?_ 71164124)_(7153543 1_?)dup	GRCh37 (hg19)		NC_000002.11	Chr2	71,164,124	71,535,431

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	Copy number
nssv15774938	GRCh37: NC_000002.11:g.(?_71164124)_(71535431_?)dup	copy number gain	unknown	not provided	Uncertain significance	ClinVar	RCV000846600.2, VCV000685892.2	3

No genotype data were submitted for this variant

You are here: NCBI