A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038678



Internal ID21948021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8961822..9102775hg38UCSC Ensembl
chr16:9055679..9196632hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38140954
hg19140954
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606009
Samples
Known GenesC16orf72, USP7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038678
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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