A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625140



Internal ID21817187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21647332..22062458hg38UCSC Ensembl
chr19:21830134..22245260hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38415127
hg19415127
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109459
Supporting Variants
Samples
Known GenesLOC641367, ZNF100, ZNF208, ZNF257, ZNF43
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625140
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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