A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598862



Internal ID20971933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32371173..32371886hg38UCSC Ensembl
chr19:32862079..32862792hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38714
hg19714
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245899
Samples
Known GenesZNF507
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598862
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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