A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594508



Internal ID20967579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71804237..71805004hg38UCSC Ensembl
chr16:71838140..71838907hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg38768
hg19768
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241300
Samples
Known GenesAP1G1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594508
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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