A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513291



Internal ID20886633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103531301..103551900hg38UCSC Ensembl
chr14:103997638..104018237hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3820600
hg1920600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015921
Samples
Known GenesTRMT61A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513291
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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