A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519667



Internal ID20893028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76872658..76903201hg38UCSC Ensembl
chr18:74584614..74615157hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3830544
hg1930544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043898
Samples
Known GenesZNF236
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519667
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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