A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569258



Internal ID20942329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29570715..29571899hg38UCSC Ensembl
chr8:29428232..29429416hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381185
hg191185
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7306n223
Supporting Variantsnssv18277660
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569258
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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