A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585344



Internal ID346923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32302071..32309702hg38UCSC Ensembl
Outerchr6:32300711..32310156hg38UCSC Ensembl
Innerchr6:32269848..32277479hg19UCSC Ensembl
Outerchr6:32268488..32277933hg19UCSC Ensembl
Innerchr6:32377826..32385457hg18UCSC Ensembl
Outerchr6:32376466..32385911hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg389446
hg199446
hg189446
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275065
Supporting Variants
Samples
Known GenesC6orf10
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)essv2585344
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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