A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173564



Internal ID15507409
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
Samples1780854573_A
Known GenesTMEM72-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173564
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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