A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602295



Internal ID16389704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491473..32515365hg38UCSC Ensembl
Innerchr6:32459250..32483142hg19UCSC Ensembl
Innerchr6:32567228..32591120hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3823893
hg1923893
hg1823893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10500n54
Supporting Variantsnssv1054962, nssv1054963
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602295
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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