A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662873



Internal ID15399525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:32462173..32507701hg38UCSC Ensembl
InnerchrX:32480290..32525818hg19UCSC Ensembl
InnerchrX:32390211..32435739hg18UCSC Ensembl
InnerchrX:32239947..32285475hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3845529
hg1945529
hg1845529
hg1745529
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520320
Supporting Variants
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662873
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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