A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596664



Internal ID20969735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36187345..36188276hg38UCSC Ensembl
chr19:36678247..36679178hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38932
hg19932
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3500n223
Supporting Variantsnssv18247674
Samples
Known GenesZNF565
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596664
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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