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dbVar

Database of genomic structural variation

esv3873527

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:10,837

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: 107 SVs from 27 studies. See in: genome view

Remapped(Score: Perfect):75,523,923-75,534,767

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3873527	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000014.9	Chr14	75,523,927 (-4, +4)	75,534,763 (-4, +4)
esv3873527	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000014.8	Chr14	75,990,270 (-4, +4)	76,001,106 (-4, +4)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv23554897	deletion	HG02133	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,146

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv23554897	Remapped	Perfect	NC_000014.9:g.(755 23923_75523931)_(7 5534759_75534767)d el	GRCh38.p12	First Pass	NC_000014.9	Chr14	75,523,927 (-4, +4)	75,534,763 (-4, +4)
essv23554897	Submitted genomic		NC_000014.8:g.(759 90266_75990274)_(7 6001102_76001110)d el	GRCh37 (hg19)		NC_000014.8	Chr14	75,990,270 (-4, +4)	76,001,106 (-4, +4)

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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