A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520153



Internal ID15447446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:114413188..114539177hg38UCSC Ensembl
InnerchrX:113647641..113773630hg19UCSC Ensembl
InnerchrX:113553897..113679886hg18UCSC Ensembl
InnerchrX:113470621..113596610hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38125990
hg19125990
hg18125990
hg17125990
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv663064, nssv661263, nssv687735, nssv690879
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520153
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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