A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596404



Internal ID20969475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21574057..22438488hg38UCSC Ensembl
chr19:21756859..22621290hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38864432
hg19864432
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244893
Samples
Known GenesLOC641367, ZNF100, ZNF208, ZNF257, ZNF43, ZNF676, ZNF729, ZNF98
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596404
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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