A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555021



Internal ID20928110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57676145..57677028hg38UCSC Ensembl
chr3:57661872..57662755hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38884
hg19884
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261547
Samples
Known GenesDENND6A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555021
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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