A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516221



Internal ID15096828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33087084..33118074hg38UCSC Ensembl
Innerchr6:33054861..33085851hg19UCSC Ensembl
Innerchr6:33162839..33193829hg18UCSC Ensembl
Innerchr6:33162839..33193829hg17UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3830991
hg1930991
hg1830991
hg1730991
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv681345, nssv680983, nssv666882, nssv696796, nssv673411, nssv662088
Samples
Known GenesHLA-DPB1, HLA-DPB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516221
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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