A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2586133



Internal ID347712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:25519366..25519396hg38UCSC Ensembl
Outerchr7:25516483..25520892hg38UCSC Ensembl
Innerchr7:25558986..25559016hg19UCSC Ensembl
Outerchr7:25556103..25560512hg19UCSC Ensembl
Innerchr7:25525511..25525541hg18UCSC Ensembl
Outerchr7:25522628..25527037hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg384410
hg194410
hg184410
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275528
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)essv2586133
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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