A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973237



Internal ID22748172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52483146..52730869hg38UCSC Ensembl
chr19:52986399..53234122hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38247724
hg19247724
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394405
Samples
Known GenesZNF137P, ZNF578, ZNF611, ZNF701, ZNF808, ZNF83
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973237
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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