A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032785



Internal ID21942128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31174102..31175239hg38UCSC Ensembl
chr16:31185423..31186560hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381138
hg191138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626312
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032785
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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