A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830412



Internal ID22605347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60211015..60219327hg38UCSC Ensembl
chr1:60676687..60684999hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg388313
hg198313
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480135
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830412
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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