A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562960



Internal ID20936031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132324040..132324805hg38UCSC Ensembl
chr3:132042884..132043649hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38766
hg19766
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260252
Samples
Known GenesACPP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562960
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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