A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563955



Internal ID336880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:118881078..118887063hg38UCSC Ensembl
chr5:118216773..118222758hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg385986
hg195986
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16973813
Samples
Known GenesDTWD2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563955
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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