A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524155



Internal ID15451448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:55481666..55662741hg38UCSC Ensembl
InnerchrX:55508099..55689174hg19UCSC Ensembl
InnerchrX:55524824..55705899hg18UCSC Ensembl
InnerchrX:55391120..55572195hg17UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg38181076
hg19181076
hg18181076
hg17181076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700034
Samples
Known GenesFOXR2, USP51
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524155
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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