A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571556



Internal ID20944627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:125047473..125049293hg38UCSC Ensembl
chr8:126059715..126061535hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg381821
hg191821
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276170
Samples
Known GenesKIAA0196
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571556
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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