A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067419



Internal ID21976652
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 StatusM
Merged Variants
Supporting Variantsnssv17567103
Samples
Known GenesSLC34A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067419
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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