A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352000



Internal ID22577669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:208793081..208800521hg38UCSC Ensembl
chr1:208966426..208973866hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg387441
hg197441
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974803
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352000
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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