A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519012



Internal ID15446305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:37975915..38053022hg38UCSC Ensembl
InnerchrX:37835168..37912275hg19UCSC Ensembl
InnerchrX:37720112..37797219hg18UCSC Ensembl
InnerchrX:37591385..37668492hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3877108
hg1977108
hg1877108
hg1777108
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696480
Samples
Known GenesCXorf27, SYTL5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519012
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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