A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521465



Internal ID15448758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:120799484..120824485hg38UCSC Ensembl
InnerchrX:119933338..119958339hg19UCSC Ensembl
InnerchrX:119817366..119842367hg18UCSC Ensembl
InnerchrX:119715220..119740221hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3825002
hg1925002
hg1825002
hg1725002
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698076
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521465
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