A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3935194



Internal ID21355263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75032863..75032863hg38UCSC Ensembl
chr14:75499566..75499566hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194867
SamplesHG002
Known GenesMLH3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3935194
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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