A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518656



Internal ID15099263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:7777235..8379574hg38UCSC Ensembl
InnerchrX:7745276..8347615hg19UCSC Ensembl
InnerchrX:7705276..8307615hg18UCSC Ensembl
InnerchrX:7555012..8157351hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38602340
hg19602340
hg18602340
hg17602340
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv499n21
Supporting Variantsnssv696105
Samples
Known GenesMIR651, PNPLA4, VCX, VCX2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518656
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