A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523140



Internal ID15450433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:145273019..145304209hg38UCSC Ensembl
InnerchrX:144354539..144385728hg19UCSC Ensembl
InnerchrX:144162231..144193420hg18UCSC Ensembl
InnerchrX:144060085..144091274hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3831191
hg1931190
hg1831190
hg1731190
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698847
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523140
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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