A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558354



Internal ID21882709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178900564..178900564hg38UCSC Ensembl
chr5:178327565..178327565hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6067040
Supporting Variants
Samples
Known GenesZFP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558354
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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