A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520001



Internal ID15100608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:96771152..97032843hg38UCSC Ensembl
Innerchr9:99533434..99795125hg19UCSC Ensembl
Innerchr9:98573255..98834946hg18UCSC Ensembl
Innerchr9:96612989..96874680hg17UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38261692
hg19261692
hg18261692
hg17261692
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv693976, nssv683518, nssv660024, nssv673014, nssv660577
Samples
Known GenesCTSV, HIATL2, LOC100132781, LOC441454, NUTM2G, ZNF510, ZNF782
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520001
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer