A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572191



Internal ID20945262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185014957..185108883hg38UCSC Ensembl
chr3:184732745..184826671hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg3893927
hg1993927
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260597
Samples
Known GenesC3orf70, VPS8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572191
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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