A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018043



Internal ID19107260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32480352..32550980hg38UCSC Ensembl
Innerchr6:32448129..32518757hg19UCSC Ensembl
Innerchr6:32556107..32626735hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3870629
hg1970629
hg1870629
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5949n100
Supporting Variantsnssv3655925, nssv3655924, nssv3655927, nssv3655930, nssv3655926, nssv3655928, nssv3655922, nssv3655921, nssv3655923, nssv3655929
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)nsv1018043
Frequency
Sample Size11257
Observed Gain4
Observed Loss6
Observed Complex0
Frequencyn/a


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