A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5827980



Internal ID22602915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13906696..13915890hg38UCSC Ensembl
chr1:14233191..14242385hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg389195
hg199195
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454355
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5827980
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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