A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568679



Internal ID16009402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:29119123..29126370hg38UCSC Ensembl
Innerchr15:29411326..29418573hg19UCSC Ensembl
Innerchr15:27198618..27205865hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg387248
hg197248
hg187248
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839310
Samples
Known GenesFAM189A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568679
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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