A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599122



Internal ID20972193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38415064..38418338hg38UCSC Ensembl
chr19:38905704..38908978hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg383275
hg193275
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248370
Samples
Known GenesRASGRP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599122
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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