A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695350



Internal ID15085316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:15296656..15331048hg38UCSC Ensembl
InnerchrX:15314778..15349170hg19UCSC Ensembl
InnerchrX:15224699..15259091hg18UCSC Ensembl
InnerchrX:15074435..15108827hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3834393
hg1934393
hg1834393
hg1734393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517938
Supporting Variants
Samples
Known GenesASB11, PIGA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695350
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