A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977059



Internal ID22751994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51091068..51091915hg38UCSC Ensembl
chr20:49707605..49708452hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38848
hg19848
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17403952
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977059
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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