A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839721



Internal ID15786991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32196903..32569140hg38UCSC Ensembl
Innerchr15:32489104..32861341hg19UCSC Ensembl
Innerchr15:30276396..30648633hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38372238
hg19372238
hg18372238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568872
Supporting Variants
Samples
Known GenesGOLGA8K, GOLGA8O, LOC100996255, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv839721
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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