A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624069



Internal ID21816116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56425426..56425426hg38UCSC Ensembl
chr16:56459338..56459338hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6088634
Supporting Variants
Samples
Known GenesAMFR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624069
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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