A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508147



Internal ID20881445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57545118..57560048hg38UCSC Ensembl
chr16:57579030..57593960hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3814931
hg1914931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029797
Samples
Known GenesGPR114
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508147
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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