A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598307



Internal ID20971378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37724308..37724695hg38UCSC Ensembl
chr19:38215209..38215596hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38388
hg19388
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3506n223
Supporting Variantsnssv18248344
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598307
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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