A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526381



Internal ID15106988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:26636293..27086968hg38UCSC Ensembl
InnerchrX:26654410..27105085hg19UCSC Ensembl
InnerchrX:26564331..27015006hg18UCSC Ensembl
InnerchrX:26414067..26864742hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38450676
hg19450676
hg18450676
hg17450676
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702678
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526381
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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