A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570563



Internal ID16357972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:95167521..95228595hg38UCSC Ensembl
Innerchr15:95710750..95771824hg19UCSC Ensembl
Innerchr15:93511754..93572828hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3861075
hg1961075
hg1861075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149619
SamplesHGDP01307
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570563
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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