A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842005



Internal ID22616940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2151104..2153529hg38UCSC Ensembl
chr5:2151218..2153643hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg382426
hg192426
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499081
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842005
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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