A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043997



Internal ID20611037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75033725..75034110hg38UCSC Ensembl
chr18:72745681..72746066hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38386
hg19386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519720
Supporting Variants
Samples
Known GenesZNF407
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00028


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