A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101736



Internal ID21483624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61969948..61969948hg38UCSC Ensembl
chr18:59637181..59637181hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653937
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101736
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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