A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508799



Internal ID20882103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85111798..85119202hg38UCSC Ensembl
chr16:85145404..85152808hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg387405
hg197405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033094
Samples
Known GenesFAM92B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508799
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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