A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979564



Internal ID12980388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57815934..58007734hg38UCSC Ensembl
Innerchr10:59575694..59767494hg19UCSC Ensembl
Innerchr10:59245700..59437500hg18UCSC Ensembl
Innerchr10:59245700..59437500hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38191801
hg19191801
hg18191801
hg17191801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35063
Supporting Variants
SamplesNA18572
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979564
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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