A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972159



Internal ID22747094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42503836..42518894hg38UCSC Ensembl
chr7:42543435..42558493hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3815059
hg1915059
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442000
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972159
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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