A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517286



Internal ID15444579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:97741654..97847091hg38UCSC Ensembl
InnerchrX:96996653..97102089hg19UCSC Ensembl
InnerchrX:96883309..96988745hg18UCSC Ensembl
InnerchrX:96802798..96908234hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38105438
hg19105437
hg18105437
hg17105437
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv678980, nssv678996, nssv676651, nssv667786, nssv659698, nssv654202, nssv654819, nssv654558, nssv658401, nssv661623, nssv693223, nssv681708, nssv685683, nssv672153, nssv679634, nssv666984, nssv678547, nssv681206, nssv690770, nssv664701
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517286
Frequency
Sample Size2026
Observed Gain13
Observed Loss7
Observed Complex0
Frequencyn/a


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