A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517085



Internal ID15444378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:147019522..147050756hg38UCSC Ensembl
InnerchrX:146101040..146132274hg19UCSC Ensembl
InnerchrX:145908732..145939966hg18UCSC Ensembl
InnerchrX:145806586..145837820hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3831235
hg1931235
hg1831235
hg1731235
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv681518, nssv653586, nssv681387
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517085
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