A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687079



Internal ID15423731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:32307648..32358828hg38UCSC Ensembl
InnerchrX:32325765..32376945hg19UCSC Ensembl
InnerchrX:32235686..32286866hg18UCSC Ensembl
InnerchrX:32085422..32136602hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3851181
hg1951181
hg1851181
hg1751181
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516788
Supporting Variants
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687079
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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