A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909919



Internal ID7385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:6345878..6346894hg38UCSC Ensembl
chr2:6486010..6487026hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5443861
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16909919
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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