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dbVar

Database of genomic structural variation

esv3902139

Organism: Homo sapiens

Study:estd225 (Magnusson et al. 2016)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:64,612

Publication(s):Magnusson et al. 2016

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: 695 SVs from 78 studies. See in: genome view

Remapped(Score: Perfect):111,031,815-111,096,426

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3902139	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000013.11	Chr13	111,031,815	111,096,426
esv3902139	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000013.10	Chr13	111,684,162	111,748,773

Variant Call Information

Variant Call ID	Type	Method	Analysis	Copy number
essv25821230	copy number gain	SNP array	SNP genotyping analysis	3

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv25821230	Remapped	Perfect	NC_000013.11:g.111 031815_111096426du p	GRCh38.p12	First Pass	NC_000013.11	Chr13	111,031,815	111,096,426
essv25821230	Submitted genomic		NC_000013.10:g.111 684162_111748773du p	GRCh37 (hg19)		NC_000013.10	Chr13	111,684,162	111,748,773

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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