A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517791



Internal ID15445084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:151990304..152104719hg38UCSC Ensembl
InnerchrX:151158776..151273191hg19UCSC Ensembl
InnerchrX:150909432..151023847hg18UCSC Ensembl
InnerchrX:150829344..150943759hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38114416
hg19114416
hg18114416
hg17114416
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699929, nssv666842, nssv653273, nssv696337, nssv664057, nssv669293, nssv684382, nssv661620, nssv654980
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517791
Frequency
Sample Size2026
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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