A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18164906



Internal ID20731946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:126342101..126345200hg38UCSC Ensembl
chr8:127354346..127357445hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418290
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18164906
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00137


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