A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521392



Internal ID15448685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:3290071..3295870hg38UCSC Ensembl
InnerchrX:3208112..3213911hg19UCSC Ensembl
InnerchrX:3218112..3223911hg18UCSC Ensembl
InnerchrX:3201473..3207272hg17UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg385800
hg195800
hg185800
hg175800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698002
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521392
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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