A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015397



Internal ID19104614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32461817..32550980hg38UCSC Ensembl
Innerchr6:32429594..32518757hg19UCSC Ensembl
Innerchr6:32537572..32626735hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3889164
hg1989164
hg1889164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5946n100
Supporting Variantsnssv3655908, nssv3655907
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)nsv1015397
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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