A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554361



Internal ID327551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9218180..9219989hg38UCSC Ensembl
chr16:9312037..9313846hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg381810
hg191810
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706914
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554361
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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