A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524166



Internal ID15451459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:121093648..121111680hg38UCSC Ensembl
InnerchrX:120227502..120245534hg19UCSC Ensembl
InnerchrX:120055183..120073215hg18UCSC Ensembl
InnerchrX:119953037..119971069hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3818033
hg1918033
hg1818033
hg1718033
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700045
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524166
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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