A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083621



Internal ID21435764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75032863..75032863hg38UCSC Ensembl
chr14:75499566..75499566hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5647348
Supporting Variants
SamplesHG00731
Known GenesMLH3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083621
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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