A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17127510



Internal ID21407117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38081361..38081709hg38UCSC Ensembl
chr3:38122852..38123200hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574342
Supporting Variants
SamplesHG00512
Known GenesDLEC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17127510
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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