A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602528



Internal ID16389937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32554371..32556447hg38UCSC Ensembl
Innerchr6:32522148..32524224hg19UCSC Ensembl
Innerchr6:32630126..32632202hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg382077
hg192077
hg182077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10555n54
Supporting Variantsnssv1055784, nssv1055773, nssv1055776, nssv1055790, nssv1055777, nssv1055774, nssv1055775, nssv1055792, nssv1055786, nssv1055780, nssv1055783, nssv1055779, nssv1055771, nssv1055787, nssv1055788, nssv1055781, nssv1055772, nssv1055789, nssv1055785, nssv1055782, nssv1055778, nssv1055791, nssv1055793
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602528
Frequency
Sample Size17421
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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