A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563007



Internal ID20936078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11106567..11107245hg38UCSC Ensembl
chr8:10964077..10964755hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276944
Samples
Known GenesXKR6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563007
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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