A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019273



Internal ID19108491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32481746..32550980hg38UCSC Ensembl
Innerchr6:32449523..32518757hg19UCSC Ensembl
Innerchr6:32557501..32626735hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3869235
hg1969235
hg1869235
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5949n100
Supporting Variantsnssv3745382, nssv3745383, nssv3655995, nssv3655996, nssv3655997, nssv3655994, nssv3745381
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019273
Frequency
Sample Size11257
Observed Gain4
Observed Loss3
Observed Complex0
Frequencyn/a


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