A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151241



Internal ID21512725
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 StatusS
Merged Variantsnsv5667151
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151241
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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