A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585147



Internal ID346726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:6857075..6859093hg38UCSC Ensembl
Outerchr6:6857036..6860514hg38UCSC Ensembl
Innerchr6:6857308..6859326hg19UCSC Ensembl
Outerchr6:6857269..6860747hg19UCSC Ensembl
Innerchr6:6802307..6804325hg18UCSC Ensembl
Outerchr6:6802268..6805746hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg383479
hg193479
hg183479
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275441
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)essv2585147
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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