A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989179



Internal ID12635828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31445144..31479044hg38UCSC Ensembl
Innerchr6:31412921..31446821hg19UCSC Ensembl
Innerchr6:31520900..31554800hg18UCSC Ensembl
Innerchr6:31520900..31554800hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3833901
hg1933901
hg1833901
hg1733901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34376
Supporting Variants
SamplesNA19202
Known GenesHCG26, HCP5
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989179
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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