A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16968461



Internal ID46288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77431676..77431794hg38UCSC Ensembl
chr5:76727501..76727619hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555090
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16968461
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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