A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039558



Internal ID20606598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25806301..25810900hg38UCSC Ensembl
chr18:23386265..23390864hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg384600
hg194600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516089
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039558
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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