A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521365



Internal ID15101972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:134586498..134588584hg38UCSC Ensembl
InnerchrX:133720528..133722614hg19UCSC Ensembl
InnerchrX:133548194..133550280hg18UCSC Ensembl
InnerchrX:133446048..133448134hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg382087
hg192087
hg182087
hg172087
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697975
Samples
Known GenesPLAC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521365
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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