A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18166865



Internal ID20733905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40817191..40825372hg38UCSC Ensembl
chr8:40674710..40682891hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg388182
hg198182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429487
Supporting Variants
Samples
Known GenesZMAT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18166865
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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