A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699386



Internal ID15089352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:135533826..135691851hg38UCSC Ensembl
InnerchrX:134667751..134825566hg19UCSC Ensembl
InnerchrX:134495417..134653232hg18UCSC Ensembl
InnerchrX:134393271..134551086hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38158026
hg19157816
hg18157816
hg17157816
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523594
Supporting Variants
Samples
Known GenesDDX26B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699386
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