A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15195474



Internal ID21334292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:397716..397716hg38UCSC Ensembl
chr16:447716..447716hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3952692
Supporting Variants
SamplesHG002
Known GenesNME4
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15195474
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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