A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842432



Internal ID22617367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43782950..43794736hg38UCSC Ensembl
chr5:43783052..43794838hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3811787
hg1911787
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496734
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842432
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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