A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691093



Internal ID15081059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:79975702..80019480hg38UCSC Ensembl
InnerchrX:79231201..79274979hg19UCSC Ensembl
InnerchrX:79117857..79161635hg18UCSC Ensembl
InnerchrX:79037346..79081124hg17UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3843779
hg1943779
hg1843779
hg1743779
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521266
Supporting Variants
Samples
Known GenesTBX22
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691093
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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