A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401592



Internal ID22459462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:58363341..58363341hg38UCSC Ensembl
chr2:58590476..58590476hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5952727
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401592
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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