A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030042



Internal ID21939385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10522468..10529664hg38UCSC Ensembl
chr16:10616325..10623521hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg387197
hg197197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602978
Samples
Known GenesEMP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030042
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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