A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977665



Internal ID22752600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170361236..170403314hg38UCSC Ensembl
chr4:171282387..171324465hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3842079
hg1942079
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417967
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977665
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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