A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17404198



Internal ID22462068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:58726372..58730647hg38UCSC Ensembl
chr2:58953507..58957782hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg384276
hg194276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867987
Supporting Variants
Samples
Known GenesLINC01122
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17404198
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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