A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5538037



Internal ID313206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112916193..112916193hg38UCSC Ensembl
chr13:113570507..113570507hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg383039
hg193039
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17693777
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5538037
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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