A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377204



Internal ID22435074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:53976868..54005627hg38UCSC Ensembl
chr17:52054229..52082988hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3828760
hg1928760
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978662
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377204
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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