A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667515



Internal ID15404167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:104444000..104480322hg38UCSC Ensembl
InnerchrX:103688681..103725003hg19UCSC Ensembl
InnerchrX:103575337..103611659hg18UCSC Ensembl
InnerchrX:103494826..103531148hg17UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3836323
hg1936323
hg1836323
hg1736323
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515495
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667515
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