A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556192



Internal ID20929263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98143885..98144447hg38UCSC Ensembl
chr8:99156113..99156675hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279231
Samples
Known GenesPOP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556192
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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