A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17412039



Internal ID22469909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123109835..123113620hg38UCSC Ensembl
chr6:123430980..123434765hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg383786
hg193786
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976723
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17412039
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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