A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489514



Internal ID21147067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75812747..75894716hg38UCSC Ensembl
chr14:76279090..76361059hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3881970
hg1981970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021155
Samples
Known GenesTTLL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489514
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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