A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656831



Internal ID15393483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5688580..5721710hg38UCSC Ensembl
InnerchrX:5606621..5639751hg19UCSC Ensembl
InnerchrX:5616621..5649751hg18UCSC Ensembl
InnerchrX:5466357..5499487hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3833131
hg1933131
hg1833131
hg1733131
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515922
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656831
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