A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568947



Internal ID16009670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34412954..34414401hg38UCSC Ensembl
Innerchr15:34705155..34706602hg19UCSC Ensembl
Innerchr15:32492447..32493894hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381448
hg191448
hg181448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4463n54
Supporting Variantsnssv839827
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568947
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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