A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043439



Internal ID20610479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6383376..6388102hg38UCSC Ensembl
chr18:6383375..6388101hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg384727
hg194727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530019
Supporting Variants
Samples
Known GenesL3MBTL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043439
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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