A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17100781



Internal ID21460560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:39707261..39707261hg38UCSC Ensembl
chr18:37287225..37287225hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663149
Supporting Variants
SamplesHG02818
Known GenesLINC00669
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17100781
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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