A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972003



Internal ID22746938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35388822..35390117hg38UCSC Ensembl
chr14:35858028..35859323hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg381296
hg191296
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382414
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972003
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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