A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417642



Internal ID22475512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132165589..132167549hg38UCSC Ensembl
chr6:132486729..132488689hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg381961
hg191961
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973872
Supporting Variants
Samples
Known GenesLINC01013
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417642
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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