A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18139957



Internal ID20706997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20808656..20813577hg38UCSC Ensembl
chr6:20808887..20813808hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384922
hg194922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402491
Supporting Variants
Samples
Known GenesCDKAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18139957
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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