A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704399



Internal ID15441051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:126829262..126920962hg38UCSC Ensembl
InnerchrX:125963245..126054945hg19UCSC Ensembl
InnerchrX:125790926..125882626hg18UCSC Ensembl
InnerchrX:125688780..125780480hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3891701
hg1991701
hg1891701
hg1791701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519509
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704399
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