A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373110



Internal ID22598779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:2514370..2529234hg38UCSC Ensembl
chr17:2417664..2432528hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3814865
hg1914865
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974903
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373110
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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