A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940367



Internal ID22715775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68578514..68578605hg38UCSC Ensembl
chr16:68612417..68612508hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383210
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940367
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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