A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17685907



Internal ID109573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19832915..19832951hg38UCSC Ensembl
chr13:20407055..20407091hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546119
Supporting Variants
Samples
Known GenesZMYM5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17685907
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.084356


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