A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568946



Internal ID16009669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34412954..34414267hg38UCSC Ensembl
Innerchr15:34705155..34706468hg19UCSC Ensembl
Innerchr15:32492447..32493760hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381314
hg191314
hg181314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4463n54
Supporting Variantsnssv839826
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568946
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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