A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16949895



Internal ID33943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:45933042..45951402hg38UCSC Ensembl
chr4:45935059..45953419hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3818361
hg1918361
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554813
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16949895
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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