A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583570



Internal ID20956641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71803995..71804775hg38UCSC Ensembl
chr16:71837898..71838678hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg38781
hg19781
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241299
Samples
Known GenesAP1G1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583570
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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