A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170024



Internal ID20737064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59193420..59193794hg38UCSC Ensembl
chr8:60105979..60106353hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428943
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170024
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00462


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