A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598894



Internal ID20971965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38828414..38829292hg38UCSC Ensembl
chr19:39319054..39319932hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38879
hg19879
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248379
Samples
Known GenesECH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598894
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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