A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173560



Internal ID15874304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44715242..44864035hg38UCSC Ensembl
Innerchr10:45210690..45359483hg19UCSC Ensembl
Innerchr10:44530696..44679489hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38148794
hg19148794
hg18148794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550706
Supporting Variants
SamplesHGDP00520
Known GenesTMEM72-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173560
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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