A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568755



Internal ID16009478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30637055..30675693hg38UCSC Ensembl
Innerchr15:30929258..30967896hg19UCSC Ensembl
Innerchr15:28716550..28755188hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3838639
hg1938639
hg1838639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4426n54
Supporting Variantsnssv839485
Samples
Known GenesARHGAP11B, LOC100288637
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568755
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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