A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552505



Internal ID16339914
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 StatusM
Merged Variants
Supporting Variantsnssv1174730
SamplesHGDP00543
Known GenesSTK32C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552505
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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