A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167979



Internal ID20735019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39917160..39923064hg38UCSC Ensembl
chr8:39774679..39780583hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg385905
hg195905
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432883
Supporting Variants
Samples
Known GenesIDO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167979
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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