A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511351



Internal ID15850776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32661242..32662159hg38UCSC Ensembl
Outerchr6:32660987..32663681hg38UCSC Ensembl
Innerchr6:32629019..32629936hg19UCSC Ensembl
Outerchr6:32628764..32631458hg19UCSC Ensembl
Innerchr6:32736997..32737914hg18UCSC Ensembl
Outerchr6:32736742..32739436hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg382695
hg192695
hg182695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625800
Samples1
Known GenesHLA-DQB1
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511351
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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