A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597997



Internal ID20971068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12605110..12606356hg38UCSC Ensembl
chr19:12715924..12717170hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381247
hg191247
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245072
Samples
Known GenesZNF490
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597997
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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