A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517514



Internal ID15444807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:16015985..16038223hg38UCSC Ensembl
Innerchr19:16126795..16149033hg19UCSC Ensembl
Innerchr19:15987795..16010033hg18UCSC Ensembl
Innerchr19:15987795..16010033hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3822239
hg1922239
hg1822239
hg1722239
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv200n21
Supporting Variantsnssv703815, nssv663359, nssv663648, nssv657813, nssv654497, nssv655034, nssv674340, nssv663781, nssv684526, nssv675309, nssv691188, nssv693377, nssv659101, nssv693744, nssv692123, nssv655542, nssv652245
Samples
Known GenesLINC00661, LINC00905
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517514
Frequency
Sample Size2026
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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