A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601835



Internal ID16389244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31356819..31357717hg38UCSC Ensembl
Innerchr6:31324596..31325494hg19UCSC Ensembl
Innerchr6:31432575..31433473hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38899
hg19899
hg18899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1053311
Samples
Known GenesHLA-B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601835
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