A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175053



Internal ID15533305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133452885..133554659hg38UCSC Ensembl
Innerchr10:135266389..135368163hg19UCSC Ensembl
Innerchr10:135116379..135218153hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38101775
hg19101775
hg18101775
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552697
Supporting Variants
SamplesNINDS_136
Known GenesCYP2E1, SCART1, SYCE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175053
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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