A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542620



Internal ID21866975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72122730..72122730hg38UCSC Ensembl
chr3:72171881..72171881hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6061569
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542620
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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