A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066994



Internal ID21512663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:81642914..81709530hg38UCSC Ensembl
chr1:82108599..82175215hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3866617
hg1966617
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671161
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066994
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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