A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520161



Internal ID15447454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:28901839..28920566hg38UCSC Ensembl
Innerchr19:29392746..29411473hg19UCSC Ensembl
Innerchr19:34084586..34103313hg18UCSC Ensembl
Innerchr19:34084586..34103313hg17UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3818728
hg1918728
hg1818728
hg1718728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697256
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520161
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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