A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602196



Internal ID16389605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32490403..32515365hg38UCSC Ensembl
Innerchr6:32458180..32483142hg19UCSC Ensembl
Innerchr6:32566158..32591120hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3824963
hg1924963
hg1824963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10500n54
Supporting Variantsnssv1054540
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602196
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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