A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18040375



Internal ID20607415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:23613541..23614330hg38UCSC Ensembl
chr18:21193505..21194294hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523595
Supporting Variants
Samples
Known GenesANKRD29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18040375
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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