A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17100806



Internal ID21474379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:2614483..2614483hg38UCSC Ensembl
chr18:2614482..2614482hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5657324
Supporting Variants
SamplesHG03371
Known GenesNDC80
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17100806
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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