A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17354185



Internal ID22579854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10474582..10485910hg38UCSC Ensembl
chr12:10627181..10638509hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3811329
hg1911329
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979907
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17354185
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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