A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829937



Internal ID22604872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27370372..27375605hg38UCSC Ensembl
chr1:27696863..27702096hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg385234
hg195234
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463043
Samples
Known GenesFCN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829937
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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