A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082001



Internal ID21991234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1599652..1599652hg38UCSC Ensembl
chr16:1649653..1649653hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607970
Samples
Known GenesIFT140
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082001
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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