A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843136



Internal ID22618071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:63495962..63520365hg38UCSC Ensembl
chr5:62791789..62816192hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3824404
hg1924404
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498025
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843136
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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