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dbVar

Database of genomic structural variation

nsv4673073

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:copy number variation
Method Type:Curated
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:88,441

Description:nsv4627093 from DECIPHER Consensus CNVs. For a full list of variants now included in nstd186, refer to the mapping file provided here.

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: 464 SVs from 56 studies. See in: genome view

Remapped(Score: Perfect):88,913,188-89,001,628

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4673073	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	88,913,188	89,001,628
nsv4673073	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000015.9	Chr15	89,456,419	89,544,859

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16195783	duplication	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv16195783	Remapped	Perfect	NC_000015.10:g.(?_ 88913188)_(8900162 8_?)dup	GRCh38.p12	First Pass	NC_000015.10	Chr15	88,913,188	89,001,628
nssv16195783	Submitted genomic		NC_000015.9:g.(?_8 9456419)_(89544859 _?)dup	GRCh37 (hg19)		NC_000015.9	Chr15	89,456,419	89,544,859

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv16195783	0.018	8	450

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