A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497973



Internal ID20871181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20040901..20043700hg38UCSC Ensembl
chr16:20052223..20055022hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029008
Samples
Known GenesGPR139
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497973
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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