A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169266



Internal ID20736306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:62623101..62659700hg38UCSC Ensembl
chr8:63535660..63572259hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3836600
hg1936600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6420905
Supporting Variants
Samples
Known GenesNKAIN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169266
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00028


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