A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555682



Internal ID20928753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98218833..98219693hg38UCSC Ensembl
chr8:99231061..99231921hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38861
hg19861
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7432n223
Supporting Variantsnssv18279235
Samples
Known GenesNIPAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555682
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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