A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979048



Internal ID12632868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:75795736..75912436hg38UCSC Ensembl
Innerchr10:77555494..77672194hg19UCSC Ensembl
Innerchr10:77225500..77342200hg18UCSC Ensembl
Innerchr10:77225500..77342200hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38116701
hg19116701
hg18116701
hg17116701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34687
Supporting Variants
SamplesNA12872
Known GenesC10orf11
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979048
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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