A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602111



Internal ID16042834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32438565..32465390hg38UCSC Ensembl
Innerchr6:32406342..32433167hg19UCSC Ensembl
Innerchr6:32514320..32541145hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3826826
hg1926826
hg1826826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154078
SamplesHGDP00718
Known GenesHLA-DRA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602111
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer