A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938717



Internal ID22714101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9095269..9152485hg38UCSC Ensembl
chr16:9189126..9246342hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3857217
hg1957217
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373091
Samples
Known GenesC16orf72
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938717
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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