A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17394405



Internal ID22452275
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 StatusS
Merged Variantsnsv5973237
Supporting Variants
Samples
Known GenesZNF137P, ZNF578, ZNF611, ZNF701, ZNF808, ZNF83
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17394405
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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