A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517103



Internal ID15444396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:157806587..157809867hg38UCSC Ensembl
Innerchr4:158727739..158731019hg19UCSC Ensembl
Innerchr4:158947189..158950469hg18UCSC Ensembl
Innerchr4:159085344..159088624hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg383281
hg193281
hg183281
hg173281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv661914, nssv664762, nssv689272, nssv679599, nssv681840, nssv654293, nssv692716, nssv680354, nssv692496, nssv675608, nssv685736, nssv673973, nssv653037, nssv681102, nssv671478, nssv661026, nssv652780, nssv661943, nssv668214, nssv673907, nssv663133, nssv666353, nssv679054, nssv666656, nssv653455, nssv666794, nssv653793, nssv658074, nssv688890, nssv691031, nssv683145, nssv668054, nssv693914, nssv665365
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517103
Frequency
Sample Size2026
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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