A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17100138



Internal ID21507047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12134973..12135642hg38UCSC Ensembl
chr18:12134972..12135641hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38670
hg19670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588190
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17100138
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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