A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979127



Internal ID12632984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31445184..31481492hg38UCSC Ensembl
Innerchr6:31412961..31449269hg19UCSC Ensembl
Innerchr6:31520940..31557248hg18UCSC Ensembl
Innerchr6:31520940..31557248hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3836309
hg1936309
hg1836309
hg1736309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34619
Supporting Variants
SamplesNA15510
Known GenesHCG26, HCP5
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979127
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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