A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573436



Internal ID20946507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37091361..37092155hg38UCSC Ensembl
chr8:36948879..36949673hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38795
hg19795
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7315n223
Supporting Variantsnssv18277871
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573436
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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