A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173569



Internal ID15507667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44715242..44873696hg38UCSC Ensembl
Innerchr10:45210690..45369144hg19UCSC Ensembl
Innerchr10:44530696..44689150hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38158455
hg19158455
hg18158455
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550708
Supporting Variants
Samples1780862090_A
Known GenesTMEM72-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173569
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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