A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086705



Internal ID21995938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87414203..87414203hg38UCSC Ensembl
chr16:87447809..87447809hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619504
Samples
Known GenesZCCHC14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086705
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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