A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602403



Internal ID16389812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32517715..32563968hg38UCSC Ensembl
Innerchr6:32485492..32531745hg19UCSC Ensembl
Innerchr6:32593470..32639723hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3846254
hg1946254
hg1846254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10522n54
Supporting Variantsnssv1055392, nssv1055388, nssv1055398, nssv1055393, nssv1055397, nssv1055402, nssv1055399, nssv1055391, nssv1055400, nssv1055394, nssv1055396, nssv1055389, nssv1055401, nssv1055390, nssv1055395
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)nsv602403
Frequency
Sample Size17421
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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