A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969135



Internal ID22744070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155390428..155448708hg38UCSC Ensembl
chr4:156311580..156369860hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3858281
hg1958281
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423471
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969135
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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