A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261544



Internal ID20828584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57669189..57669600hg38UCSC Ensembl
chr3:57654916..57655327hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550270
Supporting Variants
Samples
Known GenesDENND6A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261544
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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