A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693454



Internal ID15430106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5684069..5734525hg38UCSC Ensembl
InnerchrX:5602110..5652566hg19UCSC Ensembl
InnerchrX:5612110..5662566hg18UCSC Ensembl
InnerchrX:5461846..5512302hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3850457
hg1950457
hg1850457
hg1750457
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515922
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693454
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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