A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547811



Internal ID20921011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100800610..100800894hg38UCSC Ensembl
chr3:100519454..100519738hg19UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258877
Samples
Known GenesABI3BP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547811
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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