A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697129



Internal ID15087095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:94408340..94732102hg38UCSC Ensembl
InnerchrX:93663339..93987101hg19UCSC Ensembl
InnerchrX:93549995..93873757hg18UCSC Ensembl
InnerchrX:93469484..93793246hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38323763
hg19323763
hg18323763
hg17323763
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519792
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697129
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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