A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667151



Internal ID21615458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:54220535..54321664hg38UCSC Ensembl
chr7:54288228..54389357hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38101130
hg19101130
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151241
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667151
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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