A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169372



Internal ID20736412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65860382..65860924hg38UCSC Ensembl
chr8:66772617..66773159hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38543
hg19543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433128
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169372
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0005


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