A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842488



Internal ID22617423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177683999..177703166hg38UCSC Ensembl
chr5:177111000..177130167hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3819168
hg1919168
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498388
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842488
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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