A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16915060



Internal ID10785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68178496..68178534hg38UCSC Ensembl
chr2:68405628..68405666hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5550958
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16915060
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.043709


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