A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17100157



Internal ID21471249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12433056..12433116hg38UCSC Ensembl
chr18:12433055..12433115hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590198
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17100157
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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