A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602178



Internal ID16389587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32487705..32578039hg38UCSC Ensembl
Innerchr6:32455482..32545816hg19UCSC Ensembl
Innerchr6:32563460..32653794hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3890335
hg1990335
hg1890335
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10506n54
Supporting Variantsnssv1054495, nssv1054491, nssv1054490, nssv1054493, nssv1054494, nssv1054492, nssv1054489
Samples
Known GenesHLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602178
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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