A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506360



Internal ID20879639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19868201..19869100hg38UCSC Ensembl
chr16:19879523..19880422hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028172
Samples
Known GenesGPRC5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506360
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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