A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174730



Internal ID15874460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132256106..132291357hg38UCSC Ensembl
Innerchr10:134069610..134104861hg19UCSC Ensembl
Innerchr10:133919600..133954851hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3835252
hg1935252
hg1835252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552505
Supporting Variants
SamplesHGDP00543
Known GenesSTK32C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174730
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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