A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935699



Internal ID22711044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75120872..75123724hg38UCSC Ensembl
chr16:75154770..75157622hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg382853
hg192853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389222
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935699
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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