A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516480



Internal ID15443773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:33373627..33503133hg38UCSC Ensembl
InnerchrX:33391744..33521250hg19UCSC Ensembl
InnerchrX:33301665..33431171hg18UCSC Ensembl
InnerchrX:33151401..33280907hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38129507
hg19129507
hg18129507
hg17129507
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv509n21
Supporting Variantsnssv684040, nssv698590, nssv668609
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516480
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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