A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350622



Internal ID22576291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1604512..1608762hg38UCSC Ensembl
chr12:1713678..1717928hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg384251
hg194251
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975447
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350622
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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