A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021476



Internal ID21930819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88009617..88009677hg38UCSC Ensembl
chr16:88043223..88043283hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624117
Samples
Known GenesBANP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021476
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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