A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663635



Internal ID15400287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:98113831..98327546hg38UCSC Ensembl
InnerchrX:97368829..97582544hg19UCSC Ensembl
InnerchrX:97255485..97469200hg18UCSC Ensembl
InnerchrX:97174974..97388689hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38213716
hg19213716
hg18213716
hg17213716
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520216
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663635
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