A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486692



Internal ID21144245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75726322..75745627hg38UCSC Ensembl
chr14:76192665..76211970hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3819306
hg1919306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021148
Samples
Known GenesTTLL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486692
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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