A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674965



Internal ID15411617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:74329492..74349641hg38UCSC Ensembl
InnerchrX:73549327..73569476hg19UCSC Ensembl
InnerchrX:73466052..73486201hg18UCSC Ensembl
InnerchrX:73332348..73352497hg17UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3820150
hg1920150
hg1820150
hg1720150
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520605
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674965
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