A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602203



Internal ID16389612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32490550..32526013hg38UCSC Ensembl
Innerchr6:32458327..32493790hg19UCSC Ensembl
Innerchr6:32566305..32601768hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3835464
hg1935464
hg1835464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10501n54
Supporting Variantsnssv1054581
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602203
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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