A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135405



Internal ID20702446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111355633..111356168hg38UCSC Ensembl
chr6:111676836..111677371hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613924
Supporting Variants
Samples
Known GenesREV3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135405
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00107


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