A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044094



Internal ID20611135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:828613..871967hg38UCSC Ensembl
chr18:828614..871968hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3843355
hg1943355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517136
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044094
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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