A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974178



Internal ID22749113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68804248..68804375hg38UCSC Ensembl
chr17:66800389..66800516hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386587
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974178
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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