A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18168204



Internal ID20735244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32152999..32153531hg38UCSC Ensembl
chr8:32010515..32011047hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429648
Supporting Variants
Samples
Known GenesNRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18168204
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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