A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686516



Internal ID15423168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:32319433..32338204hg38UCSC Ensembl
InnerchrX:32337550..32356321hg19UCSC Ensembl
InnerchrX:32247471..32266242hg18UCSC Ensembl
InnerchrX:32097207..32115978hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3818772
hg1918772
hg1818772
hg1718772
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)nssv686516
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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