A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17398284



Internal ID22456154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:95666673..95918761hg38UCSC Ensembl
chr2:96332421..96584509hg19UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg38252089
hg19252089
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973264
Supporting Variants
Samples
Known GenesLINC00342
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17398284
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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