A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602496



Internal ID16389905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32551331..32553245hg38UCSC Ensembl
Innerchr6:32519108..32521022hg19UCSC Ensembl
Innerchr6:32627086..32629000hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg381915
hg191915
hg181915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10547n54
Supporting Variantsnssv1055701
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602496
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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