A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538743



Internal ID20912057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77262946..77263941hg38UCSC Ensembl
chr3:77312097..77313092hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38996
hg19996
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4926n223
Supporting Variantsnssv18262289
Samples
Known GenesROBO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538743
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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