A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5595112



Internal ID21543714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61511647..61511991hg38UCSC Ensembl
chr16:61545551..61545895hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085442
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5595112
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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