A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547136



Internal ID20920342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49067735..49068635hg38UCSC Ensembl
chr3:49105168..49106068hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262196
Samples
Known GenesQRICH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547136
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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