A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526380



Internal ID15106987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:23422570..23548414hg38UCSC Ensembl
InnerchrX:23440687..23566531hg19UCSC Ensembl
InnerchrX:23350608..23476452hg18UCSC Ensembl
InnerchrX:23200344..23326188hg17UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38125845
hg19125845
hg18125845
hg17125845
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702677
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526380
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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