A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652140



Internal ID21600445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76945283..76945283hg38UCSC Ensembl
chr18:74657239..74657239hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38824
hg19824
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17102104
SamplesHG01596
Known GenesZNF236
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652140
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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