A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518029



Internal ID15445322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:37930729..38138761hg38UCSC Ensembl
InnerchrX:37789982..37998014hg19UCSC Ensembl
InnerchrX:37674926..37882958hg18UCSC Ensembl
InnerchrX:37546199..37754231hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38208033
hg19208033
hg18208033
hg17208033
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695439
Samples
Known GenesCXorf27, SYTL5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518029
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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