A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv760498



Internal ID16054454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:127176992..127190834hg38UCSC Ensembl
Innerchr10:128975256..128989098hg19UCSC Ensembl
Innerchr10:128865246..128879088hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3813843
hg1913843
hg1813843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552299
Supporting Variants
Samples
Known GenesDOCK1, FAM196A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv760498
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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