A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842634



Internal ID22617569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:23048725..23051299hg38UCSC Ensembl
chr5:23048834..23051408hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg382575
hg192575
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495738
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842634
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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