A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599028



Internal ID20972099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43336502..43397635hg38UCSC Ensembl
chr19:43840654..43901787hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3861134
hg1961134
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246321
Samples
Known GenesCD177, PRG1, TEX101
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599028
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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