A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517098



Internal ID15444391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:28901839..28909985hg38UCSC Ensembl
Innerchr19:29392746..29400892hg19UCSC Ensembl
Innerchr19:34084586..34092732hg18UCSC Ensembl
Innerchr19:34084586..34092732hg17UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg388147
hg198147
hg188147
hg178147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664217, nssv669451, nssv674025, nssv660590, nssv692543, nssv690736, nssv681528, nssv654209, nssv653779, nssv677869, nssv652136, nssv652429, nssv666420, nssv660687, nssv674561, nssv666556, nssv664981, nssv681392, nssv679047, nssv678191, nssv678646, nssv665995, nssv656972
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517098
Frequency
Sample Size2026
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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