A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585337



Internal ID346916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:108535897..108536519hg38UCSC Ensembl
Outerchr7:108532679..108539062hg38UCSC Ensembl
Innerchr7:108176341..108176963hg19UCSC Ensembl
Outerchr7:108173123..108179506hg19UCSC Ensembl
Innerchr7:107963577..107964199hg18UCSC Ensembl
Outerchr7:107960359..107966742hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg386384
hg196384
hg186384
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275106
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)essv2585337
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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