A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595802



Internal ID20968873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43830622..43831705hg38UCSC Ensembl
chr19:44334774..44335857hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg381084
hg191084
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3665n223
Supporting Variantsnssv18246332
Samples
Known GenesZNF283
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595802
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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