A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830399



Internal ID22605334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:54898239..54903485hg38UCSC Ensembl
chr1:55363912..55369158hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg385247
hg195247
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481056
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830399
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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