A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671225



Internal ID21619530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:124425561..124546657hg38UCSC Ensembl
chr5:123761254..123882350hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38121097
hg19121097
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124835
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671225
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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