A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093570



Internal ID22002803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:74570377..74570377hg38UCSC Ensembl
chr13:75144514..75144514hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614014
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093570
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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