A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830186



Internal ID22605121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37453435..37458793hg38UCSC Ensembl
chr1:37919036..37924394hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg385359
hg195359
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467700
Samples
Known GenesLINC01137
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830186
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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