A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575465



Internal ID20948536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:125295225..125296370hg38UCSC Ensembl
chr3:125014069..125015214hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg381146
hg191146
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259529
Samples
Known GenesZNF148
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575465
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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