A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278037



Internal ID20845077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42400131..42400737hg38UCSC Ensembl
chr8:42257649..42258255hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570102
Supporting Variants
Samples
Known GenesVDAC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278037
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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