A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672439



Internal ID21620744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161373416..161476251hg38UCSC Ensembl
chr1:161343206..161446041hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38102836
hg19102836
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061254
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672439
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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