A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524538



Internal ID15105145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:75676652..75681164hg38UCSC Ensembl
Innerchr14:76142995..76147507hg19UCSC Ensembl
Innerchr14:75212748..75217260hg18UCSC Ensembl
Innerchr14:75212748..75217260hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg384513
hg194513
hg184513
hg174513
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700488
Samples
Known GenesTTLL5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524538
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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