A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18168612



Internal ID20735652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:62302801..62305900hg38UCSC Ensembl
chr8:63215360..63218459hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422954
Supporting Variants
Samples
Known GenesNKAIN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18168612
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0067


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