A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570636



Internal ID16358045
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 StatusM
Merged Variants
Supporting Variantsnssv1149160, nssv1149161
SamplesHGDP00684, HGDP00686
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570636
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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