A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17568220



Internal ID21760263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179034908..179034908hg38UCSC Ensembl
chr5:178461909..178461909hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6073649
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17568220
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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