A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536867



Internal ID20910211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38734031..38734935hg38UCSC Ensembl
chr3:38775522..38776426hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38905
hg19905
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260019
Samples
Known GenesSCN10A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536867
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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