A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18166302



Internal ID20733342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17304519..17304916hg38UCSC Ensembl
chr8:17162028..17162425hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423989
Supporting Variants
Samples
Known GenesMTMR7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18166302
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00012


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