A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18113017



Internal ID20680057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:160806342..160851354hg38UCSC Ensembl
chr4:161727494..161772506hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3845013
hg1945013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392622
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18113017
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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