A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611182



Internal ID21803229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91242240..91242240hg38UCSC Ensembl
chr13:91894494..91894494hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6095783
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611182
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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