A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602781



Internal ID16390190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32659261..32659936hg38UCSC Ensembl
Innerchr6:32627038..32627713hg19UCSC Ensembl
Innerchr6:32735016..32735691hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38676
hg19676
hg18676
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10598n54
Supporting Variantsnssv1056873, nssv1056864, nssv1056863, nssv1056862, nssv1056871, nssv1056872, nssv1056870, nssv1056865, nssv1056861, nssv1056860, nssv1056867, nssv1056866, nssv1056869, nssv1056868
Samples
Known GenesHLA-DQB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602781
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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