A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17554573



Internal ID21878928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77586986..77586986hg38UCSC Ensembl
chr5:76882811..76882811hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6071511
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17554573
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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