A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521854



Internal ID15449147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:22649874..22666244hg38UCSC Ensembl
InnerchrX:22667991..22684361hg19UCSC Ensembl
InnerchrX:22577912..22594282hg18UCSC Ensembl
InnerchrX:22427648..22444018hg17UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3816371
hg1916371
hg1816371
hg1716371
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694628
Samples
Known GenesLOC100873065
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521854
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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