A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103377



Internal ID21428035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17315107..17315240hg38UCSC Ensembl
chr19:17425916..17426049hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603134
Supporting Variants
SamplesHG00731
Known GenesDDA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103377
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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