A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560912



Internal ID333906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88306804..88309078hg38UCSC Ensembl
chr5:87602621..87604895hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg382275
hg192275
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16968840
Samples
Known GenesTMEM161B-AS1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560912
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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