A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137153



Internal ID20704193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116495839..116496523hg38UCSC Ensembl
chr6:116817002..116817686hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38685
hg19685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604943
Supporting Variants
Samples
Known GenesTRAPPC3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137153
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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