A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149160



Internal ID15875441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:97367123..97532490hg38UCSC Ensembl
Innerchr15:97910353..98075720hg19UCSC Ensembl
Innerchr15:95711357..95876724hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38165368
hg19165368
hg18165368
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570636
Supporting Variants
SamplesHGDP00684
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149160
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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