A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988036



Internal ID12979012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121672332..121701392hg38UCSC Ensembl
Innerchr10:123431846..123460906hg19UCSC Ensembl
Innerchr10:123421836..123450896hg18UCSC Ensembl
Innerchr10:123421836..123450896hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3829061
hg1929061
hg1829061
hg1729061
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 Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988036
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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