A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3948383



Internal ID21368452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:72719393..72719698hg38UCSC Ensembl
chr16:72753292..72753597hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15175605
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3948383
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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