A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842065



Internal ID22617000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155107292..155122720hg38UCSC Ensembl
chr5:154486852..154502280hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3815429
hg1915429
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496352
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842065
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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