A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18116921



Internal ID20683961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35860881..35868034hg38UCSC Ensembl
chr4:35862503..35869656hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg387154
hg197154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362546
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18116921
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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