A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524567



Internal ID15451860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:138870415..138994778hg38UCSC Ensembl
InnerchrX:137952577..138076940hg19UCSC Ensembl
InnerchrX:137780243..137904606hg18UCSC Ensembl
InnerchrX:137678097..137802460hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38124364
hg19124364
hg18124364
hg17124364
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700522
Samples
Known GenesFGF13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524567
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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