A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17104387



Internal ID21452902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31636915..31637005hg38UCSC Ensembl
chr19:32127821..32127911hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588998
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17104387
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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