A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528560



Internal ID15109167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:17329494..17484959hg38UCSC Ensembl
InnerchrX:17347617..17503082hg19UCSC Ensembl
InnerchrX:17257538..17413003hg18UCSC Ensembl
InnerchrX:17107274..17262739hg17UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38155466
hg19155466
hg18155466
hg17155466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv503n21
Supporting Variantsnssv705176
Samples
Known GenesMIR4768, NHS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528560
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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