A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519535



Internal ID15100142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19760441..20447554hg38UCSC Ensembl
Innerchr19:19871250..20630360hg19UCSC Ensembl
Innerchr19:19732250..20422200hg18UCSC Ensembl
Innerchr19:19732250..20422200hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38687114
hg19759111
hg18689951
hg17689951
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696906
Samples
Known GenesLINC00663, MIR1270-1, MIR1270-2, ZNF253, ZNF486, ZNF506, ZNF682, ZNF826P, ZNF90, ZNF93
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519535
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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