A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653269



Internal ID15389921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:112441499..112473564hg38UCSC Ensembl
InnerchrX:111684727..111716792hg19UCSC Ensembl
InnerchrX:111571383..111603448hg18UCSC Ensembl
InnerchrX:111490872..111522937hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3832066
hg1932066
hg1832066
hg1732066
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517690
Supporting Variants
Samples
Known GenesZCCHC16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653269
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