A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162632



Internal ID20729672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103565316..103565945hg38UCSC Ensembl
chr8:104577544..104578173hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415877
Supporting Variants
Samples
Known GenesRIMS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162632
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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