A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019734



Internal ID19108952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32480352..32541494hg38UCSC Ensembl
Innerchr6:32448129..32509271hg19UCSC Ensembl
Innerchr6:32556107..32617249hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3861143
hg1961143
hg1861143
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5948n100
Supporting Variantsnssv3655919, nssv3655917, nssv3655918, nssv3655920
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)nsv1019734
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer