A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980796



Internal ID12972010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19154140..19543118hg38UCSC Ensembl
Innerchr10:19443069..19832047hg19UCSC Ensembl
Innerchr10:19483075..19872053hg18UCSC Ensembl
Innerchr10:19483075..19872053hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38388979
hg19388979
hg18388979
hg17388979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750886
Supporting Variants
SamplesBEC_16
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980796
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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