A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18113835



Internal ID20680875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18472807..18478673hg38UCSC Ensembl
chr4:18474430..18480296hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg385867
hg195867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366974
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18113835
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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