A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559668



Internal ID20932739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157664901..157670076hg38UCSC Ensembl
chr3:157382690..157387865hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg385176
hg195176
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261052
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559668
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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