A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970558



Internal ID22745493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28958885..29062216hg38UCSC Ensembl
chr4:28960507..29063838hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38103332
hg19103332
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426772
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970558
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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