A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344743



Internal ID21002296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:217823172..217825018hg38UCSC Ensembl
chr2:218687895..218689741hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg381847
hg191847
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085859
Samples
Known GenesTNS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344743
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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