A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566555



Internal ID20939626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37766878..37767852hg38UCSC Ensembl
chr8:37624396..37625370hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38975
hg19975
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277880
Samples
Known GenesPROSC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566555
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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