A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830416



Internal ID22605351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61810799..61819861hg38UCSC Ensembl
chr1:62276471..62285533hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg389063
hg199063
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481097
Samples
Known GenesINADL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830416
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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