A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519013



Internal ID15446306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:57378730..57902300hg38UCSC Ensembl
InnerchrX:57405163..57928734hg19UCSC Ensembl
InnerchrX:57421888..57945459hg18UCSC Ensembl
InnerchrX:57288184..57811755hg17UCSC Ensembl
CytobandXp11.1
Allele length
AssemblyAllele length
hg38523571
hg19523572
hg18523572
hg17523572
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv514n21
Supporting Variantsnssv696481
Samples
Known GenesFAAH2, ZXDB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519013
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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