A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16924034



Internal ID16777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:128237560..128237602hg38UCSC Ensembl
chr2:128995134..128995176hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5537178
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16924034
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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