A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568599



Internal ID16356008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:26313896..26391525hg38UCSC Ensembl
Innerchr15:26559043..26636672hg19UCSC Ensembl
Innerchr15:24110136..24187765hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3877630
hg1977630
hg1877630
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149544
SamplesHGDP01187
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568599
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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