A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526197



Internal ID15106804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:129672435..129826254hg38UCSC Ensembl
InnerchrX:128806412..128960230hg19UCSC Ensembl
InnerchrX:128634093..128787911hg18UCSC Ensembl
InnerchrX:128531947..128685765hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38153820
hg19153819
hg18153819
hg17153819
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702459
Samples
Known GenesSASH3, XPNPEP2, ZDHHC9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526197
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