A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044688



Internal ID20611728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:72671292..72676197hg38UCSC Ensembl
chr18:70338527..70343432hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg384906
hg194906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517675
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044688
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00044


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