A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598100



Internal ID20971171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21574056..23113345hg38UCSC Ensembl
chr19:21756858..23296147hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381539290
hg191539290
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3478n223
Supporting Variantsnssv18244892
Samples
Known GenesLOC100996349, LOC440518, LOC641367, ZNF100, ZNF208, ZNF257, ZNF43, ZNF492, ZNF676, ZNF728, ZNF729, ZNF98, ZNF99
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598100
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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