A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570471



Internal ID20943542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105454688..105455459hg38UCSC Ensembl
chr3:105173532..105174303hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38772
hg19772
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4968n223
Supporting Variantsnssv18259070
Samples
Known GenesALCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570471
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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