A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17414395



Internal ID22472265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46449495..46450337hg38UCSC Ensembl
chr3:46490985..46491827hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38843
hg19843
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977463
Supporting Variants
Samples
Known GenesLTF
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17414395
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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