A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662548



Internal ID21610853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76851082..76851082hg38UCSC Ensembl
chr18:74563038..74563038hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17102852
SamplesHG00731
Known GenesZNF236
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662548
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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