A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17418493



Internal ID22476363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157233942..157233942hg38UCSC Ensembl
chr5:156660952..156660952hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961940
Supporting Variants
Samples
Known GenesITK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17418493
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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