A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987361



Internal ID12981717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57142410..57177149hg38UCSC Ensembl
Innerchr10:58902170..58936909hg19UCSC Ensembl
Innerchr10:58572176..58606915hg18UCSC Ensembl
Innerchr10:58572176..58606915hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3834740
hg1934740
hg1834740
hg1734740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35059
Supporting Variants
SamplesNA18995
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987361
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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