A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035498



Internal ID21944841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81668838..81668911hg38UCSC Ensembl
chr16:81702443..81702516hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628828
Samples
Known GenesCMIP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035498
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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