A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526363



Internal ID15453656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:116468004..116776928hg38UCSC Ensembl
InnerchrX:115599165..115910896hg19UCSC Ensembl
InnerchrX:115513193..115794924hg18UCSC Ensembl
InnerchrX:115411047..115692778hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38308925
hg19311732
hg18281732
hg17281732
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702656
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526363
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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