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
hg3814349
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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