A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842556



Internal ID22617491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:20795865..20797304hg38UCSC Ensembl
chr5:20795974..20797413hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg381440
hg191440
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499069
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842556
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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