A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835853



Internal ID22610788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23722199..23752305hg38UCSC Ensembl
chr3:23763690..23793796hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3830107
hg1930107
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490946
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835853
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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