A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245885



Internal ID20812925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32032144..33117460hg38UCSC Ensembl
chr19:32523050..33608366hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381085317
hg191085317
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596670
Supporting Variants
Samples
Known GenesANKRD27, C19orf40, CEP89, DPY19L3, GPATCH1, LOC400684, NUDT19, PDCD5, RGS9BP, RHPN2, SLC7A9, TDRD12, ZNF507
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245885
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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