A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17353654



Internal ID22579323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:204001755..204006327hg38UCSC Ensembl
chr1:203970883..203975455hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg384573
hg194573
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978500
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17353654
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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