A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17100669



Internal ID21487141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:28156510..28156510hg38UCSC Ensembl
chr18:25736474..25736474hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651173
Supporting Variants
SamplesNA12878
Known GenesCDH2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17100669
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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