A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978172



Internal ID22753107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77290885..77578369hg38UCSC Ensembl
chr18:75002841..75290325hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38287485
hg19287485
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395531
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978172
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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