A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979293



Internal ID12979946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20457271..20620275hg38UCSC Ensembl
Innerchr10:20746200..20909204hg19UCSC Ensembl
Innerchr10:20786206..20949210hg18UCSC Ensembl
Innerchr10:20786206..20949210hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38163005
hg19163005
hg18163005
hg17163005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34621
Supporting Variants
SamplesNA18524
Known GenesMIR4675
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979293
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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