A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909008



Internal ID6797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5645514..5645515hg38UCSC Ensembl
chr2:5785646..5785647hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg382
hg192
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562859
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16909008
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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