A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043050



Internal ID20610090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6095289..6115936hg38UCSC Ensembl
chr18:6095288..6115935hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3820648
hg1920648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534259
Supporting Variants
Samples
Known GenesL3MBTL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043050
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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