A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391535



Internal ID21382565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23632246..23632411hg38UCSC Ensembl
chr16:23643567..23643732hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15706019
Samples
Known GenesPALB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391535
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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