A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528363



Internal ID15108970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:14115921..14251716hg38UCSC Ensembl
InnerchrX:14134040..14269838hg19UCSC Ensembl
InnerchrX:14043961..14179759hg18UCSC Ensembl
InnerchrX:13893697..14029495hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38135796
hg19135799
hg18135799
hg17135799
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv501n21
Supporting Variantsnssv704950
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528363
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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