A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892133



Internal ID22667178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156890562..156904910hg38UCSC Ensembl
chr5:156317573..156331921hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38n/a
hg1914349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429078
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892133
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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