A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043405



Internal ID20610445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63512682..63523702hg38UCSC Ensembl
chr18:61179915..61190935hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3811021
hg1911021
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522307
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043405
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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