A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563618



Internal ID336550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45335591..45337667hg38UCSC Ensembl
chr20:43964231..43966307hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg382077
hg192077
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732608
Samples
Known GenesSDC4
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563618
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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