A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990132



Internal ID12983943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19143845..19520745hg38UCSC Ensembl
Innerchr10:19432774..19809674hg19UCSC Ensembl
Innerchr10:19472780..19849680hg18UCSC Ensembl
Innerchr10:19472780..19849680hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38376901
hg19376901
hg18376901
hg17376901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750885
Supporting Variants
SamplesSPC_38
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6990132
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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