A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569657



Internal ID20942728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47319822..52044550hg38UCSC Ensembl
chr8:48232411..52957110hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg384724729
hg194724700
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278100
Samples
Known GenesC8orf22, CEBPD, EFCAB1, LOC101929217, LOC101929268, MCM4, PCMTD1, PRKDC, PXDNL, SNAI2, SNTG1, SPIDR, UBE2V2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569657
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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