A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17407621



Internal ID22465491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12208918..12209444hg38UCSC Ensembl
chr19:12319733..12320259hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38527
hg19527
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5972184
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17407621
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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