A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362799



Internal ID22588468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113411924..113412251hg38UCSC Ensembl
chr10:115171683..115172010hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971673
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362799
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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