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

dbVar

Database of genomic structural variation

nsv3901169

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:492,529

Description:GRCh37/hg19 17q12(chr17:37387413-37879941)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: 1728 SVs from 75 studies. See in: genome view

Remapped(Score: Perfect):39,231,160-39,723,688

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv3901169	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000017.11	Chr17	39,231,160	39,723,688
nsv3901169	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000017.10	Chr17	37,387,413	37,879,941

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv15160922	copy number gain	Multiple	Multiple	not provided	Benign	ClinVar	RCV000739510.2, VCV000602874.2	3

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15160922	Remapped	Perfect	NC_000017.11:g.(?_ 39231160)_(3972368 8_?)dup	GRCh38.p12	First Pass	NC_000017.11	Chr17	39,231,160	39,723,688
nssv15160922	Submitted genomic		NC_000017.10:g.(?_ 37387413)_(3787994 1_?)dup	GRCh37 (hg19)		NC_000017.10	Chr17	37,387,413	37,879,941

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
nssv15160922	GRCh37: NC_000017.10:g.(?_37387413)_(37879941_?)dup	copy number gain	unknown	not provided	Benign	ClinVar	RCV000739510.2, VCV000602874.2	3

No genotype data were submitted for this variant

You are here: NCBI