A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567884



Internal ID21759927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35664660..35664660hg38UCSC Ensembl
chr7:35704270..35704270hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6070796
Supporting Variants
Samples
Known GenesHERPUD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567884
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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