A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543938



Internal ID21868293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149130881..149130881hg38UCSC Ensembl
chr3:148848668..148848668hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6071961
Supporting Variants
Samples
Known GenesHPS3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543938
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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