A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979565



Internal ID12980387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57816163..58012428hg38UCSC Ensembl
Innerchr10:59575923..59772188hg19UCSC Ensembl
Innerchr10:59245929..59442194hg18UCSC Ensembl
Innerchr10:59245929..59442194hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38196266
hg19196266
hg18196266
hg17196266
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 Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979565
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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