A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590013



Internal ID20963084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57183041..57183576hg38UCSC Ensembl
chr16:57216953..57217488hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239315
Samples
Known GenesFAM192A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590013
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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