A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989752



Internal ID12628288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:64367133..64492237hg38UCSC Ensembl
Innerchr10:66126893..66251994hg19UCSC Ensembl
Innerchr10:65796899..65922000hg18UCSC Ensembl
Innerchr10:65796899..65922000hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38125105
hg19125102
hg18125102
hg17125102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750967
Supporting Variants
SamplesBEC_554
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989752
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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