A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977368



Internal ID22752303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19879275..19879275hg38UCSC Ensembl
chr16:19890597..19890597hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374707
Samples
Known GenesGPRC5B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977368
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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