A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657337



Internal ID18955618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32540687..32657306hg38UCSC Ensembl
Innerchr6:32508464..32625083hg19UCSC Ensembl
Innerchr6:32616442..32733061hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38116620
hg19116620
hg18116620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025310
Supporting Variants
Samples
Known GenesHLA-DQA1, HLA-DRB1, 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)nssv3657337
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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