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dbVar

Database of genomic structural variation

nsv4675391

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:4,458,767

Description:GRCh37/hg19 15q14(chr15:34197488-38656254)x1 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: 12509 SVs from 126 studies. See in: genome view

Remapped(Score: Perfect):33,905,287-38,364,053

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4675391	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	33,905,287	38,364,053
nsv4675391	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000015.9	Chr15	34,197,488	38,656,254

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv16208948	copy number loss	Multiple	Multiple	not provided	Pathogenic	ClinVar	RCV001006677.1, VCV000815702.1	1

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv16208948	Remapped	Perfect	NC_000015.10:g.(?_ 33905287)_(3836405 3_?)del	GRCh38.p12	First Pass	NC_000015.10	Chr15	33,905,287	38,364,053
nssv16208948	Submitted genomic		NC_000015.9:g.(?_3 4197488)_(38656254 _?)del	GRCh37 (hg19)		NC_000015.9	Chr15	34,197,488	38,656,254

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
nssv16208948	GRCh37: NC_000015.9:g.(?_34197488)_(38656254_?)del	copy number loss	germline	not provided	Pathogenic	ClinVar	RCV001006677.1, VCV000815702.1	1

No genotype data were submitted for this variant

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