A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552369



Internal ID20925496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57904879..57905421hg38UCSC Ensembl
chr3:57890606..57891148hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38543
hg19543
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261566
Samples
Known GenesSLMAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552369
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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