A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517194



Internal ID15444487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7169738..7201973hg38UCSC Ensembl
Innerchr5:7169851..7202086hg19UCSC Ensembl
Innerchr5:7222851..7255086hg18UCSC Ensembl
Innerchr5:7222851..7255086hg17UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3832236
hg1932236
hg1832236
hg1732236
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv686666, nssv673423, nssv678018, nssv693680, nssv679257, nssv657461, nssv688726, nssv692320, nssv687094, nssv692009, nssv677387, nssv672715, nssv653985, nssv692639, nssv672667, nssv652326, nssv692680, nssv693728, nssv680682, nssv655951, nssv677484, nssv666220, nssv689104, nssv656341, nssv659929, nssv659093, nssv654907, nssv688508, nssv675586, nssv672020, nssv683009, nssv682211, nssv672090, nssv681231, nssv659057, nssv667666, nssv689632, nssv652259, nssv692365, nssv660657
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517194
Frequency
Sample Size2026
Observed Gain0
Observed Loss40
Observed Complex0
Frequencyn/a


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