A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569597



Internal ID16010320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58125696..58165308hg38UCSC Ensembl
Innerchr15:58417895..58457507hg19UCSC Ensembl
Innerchr15:56205187..56244799hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3839613
hg1939613
hg1839613
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149224
SamplesHGDP00814
Known GenesAQP9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569597
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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