A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600025



Internal ID20973096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52249015..52249557hg38UCSC Ensembl
chr19:52752268..52752810hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38543
hg19543
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246693
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600025
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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