A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958361



Internal ID22733432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215401206..215401206hg38UCSC Ensembl
chr2:216265929..216265929hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396585
Samples
Known GenesFN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958361
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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