A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17545705



Internal ID21870060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67339325..67339325hg38UCSC Ensembl
chr5:66635153..66635153hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6076253
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17545705
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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