A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518380



Internal ID15098987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:135389912..135463380hg38UCSC Ensembl
InnerchrX:134523837..134597305hg19UCSC Ensembl
InnerchrX:134351503..134424971hg18UCSC Ensembl
InnerchrX:134249357..134322825hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3873469
hg1973469
hg1873469
hg1773469
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695811
Samples
Known GenesLINC00086, LOC100506790
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518380
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