A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174154



Internal ID15876057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20543483..20576228hg38UCSC Ensembl
Innerchr10:20832412..20865157hg19UCSC Ensembl
Innerchr10:20872418..20905163hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3832746
hg1932746
hg1832746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550161
Supporting Variants
SamplesHGDP00779
Known GenesMIR4675
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174154
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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