A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683873



Internal ID15420525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:8952896..8976062hg38UCSC Ensembl
InnerchrX:8920937..8944103hg19UCSC Ensembl
InnerchrX:8880937..8904103hg18UCSC Ensembl
InnerchrX:8730673..8753839hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3823167
hg1923167
hg1823167
hg1723167
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515590
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683873
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