A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018442



Internal ID19107659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32486734..32589524hg38UCSC Ensembl
Innerchr6:32454511..32557301hg19UCSC Ensembl
Innerchr6:32562489..32665279hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38102791
hg19102791
hg18102791
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5947n100
Supporting Variantsnssv3657312, nssv3657322, nssv3657317, nssv3657325, nssv3657328, nssv3657330, nssv3657326, nssv3657329, nssv3657318, nssv3657313, nssv3657321, nssv3657310, nssv3657320, nssv3657324, nssv3657319, nssv3745466, nssv3657327, nssv3657314, nssv3657316, nssv3657323, nssv3657311, nssv3657315
Samples
Known GenesHLA-DRB1, HLA-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)nsv1018442
Frequency
Sample Size11257
Observed Gain22
Observed Loss0
Observed Complex0
Frequencyn/a


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