A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16910567



Internal ID7817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24766599..24766601hg38UCSC Ensembl
chr2:24989468..24989470hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534085
Supporting Variants
Samples
Known GenesNCOA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16910567
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.043464


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