A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595746



Internal ID20968817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9618888..9620238hg38UCSC Ensembl
chr19:9729564..9730914hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381351
hg191351
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246556
Samples
Known GenesZNF561
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595746
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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