A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556034



Internal ID329181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180989037..181073600hg38UCSC Ensembl
chr5:180416037..180500600hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3884564
hg1984564
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16978347
Samples
Known GenesBTNL3, BTNL9, MIR8089
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556034
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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