A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579946



Internal ID20953017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57161703..57163114hg38UCSC Ensembl
chr16:57195615..57197026hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg381412
hg191412
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239313
Samples
Known GenesFAM192A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579946
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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