A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561325



Internal ID21885680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177994441..177994441hg38UCSC Ensembl
chr5:177421442..177421442hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6063526
Supporting Variants
Samples
Known GenesPROP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561325
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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