A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688968



Internal ID15425620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:87430890..87486397hg38UCSC Ensembl
InnerchrX:86685893..86741400hg19UCSC Ensembl
InnerchrX:86572549..86628056hg18UCSC Ensembl
InnerchrX:86492038..86547545hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3855508
hg1955508
hg1855508
hg1755508
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520176
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688968
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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