A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697837



Internal ID15434489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:28241793..28294683hg38UCSC Ensembl
InnerchrX:28259910..28312800hg19UCSC Ensembl
InnerchrX:28169831..28222721hg18UCSC Ensembl
InnerchrX:28019567..28072457hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3852891
hg1952891
hg1852891
hg1752891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521194
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697837
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