A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559269



Internal ID20932340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185348804..185350395hg38UCSC Ensembl
chr3:185066592..185068183hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg381592
hg191592
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260611
Samples
Known GenesMAP3K13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559269
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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