A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602269



Internal ID16389678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491135..32592550hg38UCSC Ensembl
Innerchr6:32458912..32560327hg19UCSC Ensembl
Innerchr6:32566890..32668305hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38101416
hg19101416
hg18101416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10506n54
Supporting Variantsnssv1054890, nssv1054896, nssv1054900, nssv1054899, nssv1054888, nssv1054884, nssv1054894, nssv1054889, nssv1054895, nssv1054901, nssv1054883, nssv1054892, nssv1054885, nssv1054897, nssv1054886, nssv1054893, nssv1054891, nssv1054898, nssv1054887
Samples
Known GenesHLA-DRB1, HLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602269
Frequency
Sample Size17421
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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