A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967889



Internal ID22742824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:178513923..179033063hg38UCSC Ensembl
chr4:179435077..179954217hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38519141
hg19519141
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419032
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967889
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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