A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18164136



Internal ID20731177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119086264..119086949hg38UCSC Ensembl
chr8:120098503..120099188hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425600
Supporting Variants
Samples
Known GenesCOLEC10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18164136
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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