A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842879



Internal ID22617814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7927149..7928176hg38UCSC Ensembl
chr5:7927262..7928289hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg381028
hg191028
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498743
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842879
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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