A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167994



Internal ID20735034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40104162..40104545hg38UCSC Ensembl
chr8:39961681..39962064hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424921
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167994
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00106


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