A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566505



Internal ID20939576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38184991..38185794hg38UCSC Ensembl
chr8:38042509..38043312hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38804
hg19804
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7317n223
Supporting Variantsnssv18277908
Samples
Known GenesBAG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566505
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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