A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023009



Internal ID21932352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9263787..9274182hg38UCSC Ensembl
chr16:9357644..9368039hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3810396
hg1910396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609115
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023009
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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