A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843097



Internal ID22618032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56418291..56423866hg38UCSC Ensembl
chr5:55714118..55719693hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg385576
hg195576
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497411
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843097
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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