A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173878



Internal ID15875661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:52937863..53169243hg38UCSC Ensembl
Innerchr10:54697623..54929003hg19UCSC Ensembl
Innerchr10:54367629..54599009hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38231381
hg19231381
hg18231381
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550906
Supporting Variants
SamplesHGDP00717
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173878
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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