A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509790



Internal ID20883101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85053893..85216291hg38UCSC Ensembl
chr16:85087499..85249897hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38162399
hg19162399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033082
Samples
Known GenesFAM92B, KIAA0513, LOC400548
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509790
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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