A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544819



Internal ID20918056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105454686..105455435hg38UCSC Ensembl
chr3:105173530..105174279hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38750
hg19750
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4968n223
Supporting Variantsnssv18259069
Samples
Known GenesALCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544819
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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