A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427264



Internal ID22485134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159270856..159270856hg38UCSC Ensembl
chr5:158697864..158697864hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967423
Supporting Variants
Samples
Known GenesUBLCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427264
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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