A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971286



Internal ID22746221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95947288..95982674hg38UCSC Ensembl
chr14:96413625..96449011hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3835387
hg1935387
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375498
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971286
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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