A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174137



Internal ID15532778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:16672467..16954685hg38UCSC Ensembl
Innerchr10:16714466..16996684hg19UCSC Ensembl
Innerchr10:16754472..17036690hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38282219
hg19282219
hg18282219
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550020
Supporting Variants
SamplesHGDP01370
Known GenesCUBN, RSU1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174137
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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