A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978718



Internal ID12979020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121676496..121701496hg38UCSC Ensembl
Innerchr10:123436010..123461010hg19UCSC Ensembl
Innerchr10:123426000..123451000hg18UCSC Ensembl
Innerchr10:123426000..123451000hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3825001
hg1925001
hg1825001
hg1725001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34777
Supporting Variants
SamplesNA12156
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978718
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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