A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17393361



Internal ID22451231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:8152748..8153079hg38UCSC Ensembl
chr2:8292878..8293209hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967638
Supporting Variants
Samples
Known GenesLINC00299
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17393361
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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