A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548986



Internal ID20922164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:6268151..6410269hg38UCSC Ensembl
chr3:6309838..6451956hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38142119
hg19142119
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262239
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548986
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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