A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585635



Internal ID347214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:106181400..106181400hg38UCSC Ensembl
Outerchr7:106180814..106181485hg38UCSC Ensembl
Innerchr7:105821846..105821846hg19UCSC Ensembl
Outerchr7:105821260..105821931hg19UCSC Ensembl
Innerchr7:105609082..105609082hg18UCSC Ensembl
Outerchr7:105608496..105609167hg18UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg38672
hg19672
hg18672
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275468
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)essv2585635
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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