A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520351



Internal ID15100958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:115073935..115318424hg38UCSC Ensembl
InnerchrX:114308498..114552991hg19UCSC Ensembl
InnerchrX:114214754..114459247hg18UCSC Ensembl
InnerchrX:114131478..114375971hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38244490
hg19244494
hg18244494
hg17244494
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697366
Samples
Known GenesLRCH2, LUZP4, RBMXL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520351
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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