A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16965437



Internal ID44277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:44645209..44662136hg38UCSC Ensembl
chr5:44645311..44662238hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3816928
hg1916928
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560802
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16965437
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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