A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019767



Internal ID19108985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32480352..32559495hg38UCSC Ensembl
Innerchr6:32448129..32527272hg19UCSC Ensembl
Innerchr6:32556107..32635250hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3879144
hg1979144
hg1879144
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5949n100
Supporting Variantsnssv3655935, nssv3655939, nssv3655932, nssv3655937, nssv3655931, nssv3655934, nssv3655933, nssv3655938, nssv3655936
Samples
Known GenesHLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019767
Frequency
Sample Size11257
Observed Gain7
Observed Loss2
Observed Complex0
Frequencyn/a


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