A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668749



Internal ID21617054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:63181462..63205546hg38UCSC Ensembl
chr5:62477289..62501373hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3824085
hg1924085
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144581
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668749
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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