A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596909



Internal ID20969980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11501289..11502940hg38UCSC Ensembl
chr19:11612104..11613755hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381652
hg191652
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245011
Samples
Known GenesZNF653
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596909
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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