A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567103



Internal ID21759146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177396477..177396477hg38UCSC Ensembl
chr5:176823478..176823478hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6067419
Supporting Variants
Samples
Known GenesSLC34A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567103
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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