A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17572003



Internal ID21764046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176771276..176771276hg38UCSC Ensembl
chr5:176198277..176198277hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6063627
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17572003
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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