A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517077



Internal ID15097684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:43170260..43513635hg38UCSC Ensembl
InnerchrX:43029509..43372884hg19UCSC Ensembl
InnerchrX:42914453..43257828hg18UCSC Ensembl
InnerchrX:42785763..43129138hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38343376
hg19343376
hg18343376
hg17343376
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv682761, nssv691764, nssv689478, nssv692237, nssv678039, nssv675660, nssv676366, nssv653740, nssv682192, nssv692981, nssv659346, nssv666143, nssv667957, nssv690250
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517077
Frequency
Sample Size2026
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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