A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511350



Internal ID15850775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32487705..32537953hg38UCSC Ensembl
Outerchr6:32486033..32538068hg38UCSC Ensembl
Innerchr6:32455482..32505730hg19UCSC Ensembl
Outerchr6:32453810..32505845hg19UCSC Ensembl
Innerchr6:32563460..32613708hg18UCSC Ensembl
Outerchr6:32561788..32613823hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3852036
hg1952036
hg1852036
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625788
Samples1
Known GenesHLA-DRB5
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511350
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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