A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507474



Internal ID20880766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68233076..68242756hg38UCSC Ensembl
chr16:68266979..68276659hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg389681
hg199681
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031690
Samples
Known GenesESRP2, MIR6773
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507474
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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