A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569818



Internal ID16357227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70944020..71074673hg38UCSC Ensembl
Innerchr15:71236359..71367012hg19UCSC Ensembl
Innerchr15:69023413..69154066hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38130654
hg19130654
hg18130654
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149240
SamplesHGDP00023
Known GenesLRRC49
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569818
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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