A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543682



Internal ID20916928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37046897..37047811hg38UCSC Ensembl
chr3:37088388..37089302hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38915
hg19915
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4846n223
Supporting Variantsnssv18259983
Samples
Known GenesMLH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543682
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer