A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101341



Internal ID21493301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59227004..59227004hg38UCSC Ensembl
chr18:56894236..56894236hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664525
Supporting Variants
SamplesNA19238
Known GenesGRP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101341
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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