A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567042



Internal ID20940113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9015063..9015747hg38UCSC Ensembl
chr8:8872573..8873257hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38685
hg19685
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279004
Samples
Known GenesERI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567042
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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