A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670429



Internal ID15407081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:54599382..54614994hg38UCSC Ensembl
InnerchrX:54625815..54641427hg19UCSC Ensembl
InnerchrX:54642540..54658152hg18UCSC Ensembl
InnerchrX:54508836..54524448hg17UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3815613
hg1915613
hg1815613
hg1715613
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517375
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670429
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