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dbVar

Database of genomic structural variation

esv3878073

Organism: Homo sapiens

Study:estd219 (1000 Genomes Consortium Phase 3 Integrated SV)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:64,851

Publication(s):1000 Genomes Consortium Phase 3 Integrated SV

Links to Other Resources

Overlapping Genes

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: 375 SVs from 48 studies. See in: genome view

Remapped(Score: Perfect):76,890,119-76,954,969

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3878073	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000016.10	Chr16	76,890,119	76,954,969
esv3878073	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000016.9	Chr16	76,924,016	76,988,866

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv24063566	deletion	HG03054	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,343

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv24063566	Remapped	Perfect	NC_000016.10:g.768 90119_76954969del	GRCh38.p12	First Pass	NC_000016.10	Chr16	76,890,119	76,954,969
essv24063566	Submitted genomic		NC_000016.9:g.7692 4016_76988866del	GRCh37 (hg19)		NC_000016.9	Chr16	76,924,016	76,988,866

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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