A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569389



Internal ID20942460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37877739..37878488hg38UCSC Ensembl
chr8:37735257..37736006hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38750
hg19750
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277883
Samples
Known GenesRAB11FIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569389
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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