A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556916



Internal ID20929987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:19963180..19963967hg38UCSC Ensembl
chr8:19820691..19821478hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38788
hg19788
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7295n223
Supporting Variantsnssv18277437
Samples
Known GenesLPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556916
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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