A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655834



Internal ID15392486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5688580..5743495hg38UCSC Ensembl
InnerchrX:5606621..5661536hg19UCSC Ensembl
InnerchrX:5616621..5671536hg18UCSC Ensembl
InnerchrX:5466357..5521272hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3854916
hg1954916
hg1854916
hg1754916
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)nssv655834
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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