A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17549080



Internal ID21873435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135409622..135409622hg38UCSC Ensembl
chr5:134745312..134745312hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg382732
hg192732
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6072278
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17549080
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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