A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581347



Internal ID20954418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20037233..20037923hg38UCSC Ensembl
chr16:20048555..20049245hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38691
hg19691
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239202
Samples
Known GenesGPR139
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581347
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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