A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581153



Internal ID20954224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1226139..1244738hg38UCSC Ensembl
chr16:1276139..1294739hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3818600
hg1918601
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2659n223
Supporting Variantsnssv18239873
Samples
Known GenesTPSAB1, TPSB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581153
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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