A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597506



Internal ID20970577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37336314..37336796hg38UCSC Ensembl
chr19:37827216..37827698hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248313
Samples
Known GenesHKR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597506
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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