A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516661



Internal ID15097268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:41140431..41269240hg38UCSC Ensembl
InnerchrX:40999684..41128493hg19UCSC Ensembl
InnerchrX:40884628..41013437hg18UCSC Ensembl
InnerchrX:40755938..40884747hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38128810
hg19128810
hg18128810
hg17128810
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv512n21
Supporting Variantsnssv685136, nssv700164, nssv684177, nssv659460, nssv669951, nssv676709, nssv660879, nssv679486, nssv691434, nssv686517
Samples
Known GenesUSP9X
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516661
Frequency
Sample Size2026
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer