A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517746



Internal ID15445039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:20727315..21074534hg38UCSC Ensembl
InnerchrX:20745433..21092652hg19UCSC Ensembl
InnerchrX:20655354..21002573hg18UCSC Ensembl
InnerchrX:20505090..20852309hg17UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg38347220
hg19347220
hg18347220
hg17347220
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv688460, nssv689823, nssv655419, nssv656378, nssv693591, nssv682820, nssv661855, nssv659731, nssv664573, nssv675659, nssv677048, nssv656818, nssv679390, nssv680223, nssv692462, nssv660608, nssv653087, nssv679314, nssv666142
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517746
Frequency
Sample Size2026
Observed Gain19
Observed Loss0
Observed Complex0
Frequencyn/a


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