A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602405



Internal ID16389814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32519533..32520464hg38UCSC Ensembl
Innerchr6:32487310..32488241hg19UCSC Ensembl
Innerchr6:32595288..32596219hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38932
hg19932
hg18932
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1055407, nssv1055410, nssv1055408, nssv1055406, nssv1055409
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602405
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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