A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17403588



Internal ID22461458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21647331..22062457hg38UCSC Ensembl
chr19:21830133..22245259hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38415127
hg19415127
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971480
Supporting Variants
Samples
Known GenesLOC641367, ZNF100, ZNF208, ZNF257, ZNF43
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17403588
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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