A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511316



Internal ID15504055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29882552..29907835hg38UCSC Ensembl
Outerchr6:29882497..29907959hg38UCSC Ensembl
Innerchr6:29850329..29875612hg19UCSC Ensembl
Outerchr6:29850274..29875736hg19UCSC Ensembl
Innerchr6:29958308..29983591hg18UCSC Ensembl
Outerchr6:29958253..29983715hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3825463
hg1925463
hg1825463
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625410
Samples1
Known GenesHLA-H
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511316
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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