A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5597695



Internal ID21546312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23517214..23517526hg38UCSC Ensembl
chr16:23528535..23528847hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089702
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5597695
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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