A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830323



Internal ID22605258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42879825..42896376hg38UCSC Ensembl
chr1:43345496..43362047hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3816552
hg1916552
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459164
Samples
Known GenesLOC339539
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830323
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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