A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970032



Internal ID22744967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18269893..18364433hg38UCSC Ensembl
chr4:18271516..18366056hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3894541
hg1994541
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429327
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970032
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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