A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18041998



Internal ID20609038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:48064850..48065458hg38UCSC Ensembl
chr18:45591221..45591829hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528562
Supporting Variants
Samples
Known GenesZBTB7C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18041998
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00064


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