A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5961940



Internal ID22736879
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 StatusM
Merged Variants
Supporting Variantsnssv17418493
Samples
Known GenesITK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5961940
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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