A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437805



Internal ID22495675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116854051..116854051hg38UCSC Ensembl
chr8:117866290..117866290hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5957177
Supporting Variants
Samples
Known GenesRAD21
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437805
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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