A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601968



Internal ID16389377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31903977..31910331hg38UCSC Ensembl
Innerchr6:31871754..31878108hg19UCSC Ensembl
Innerchr6:31979733..31986087hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg386355
hg196355
hg186355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10465n54
Supporting Variantsnssv1053562
Samples
Known GenesC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601968
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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