A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17549434



Internal ID21873789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68127877..68127877hg38UCSC Ensembl
chr3:68177027..68177027hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6076332
Supporting Variants
Samples
Known GenesFAM19A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17549434
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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