A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103810



Internal ID21471893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11547083..11547185hg38UCSC Ensembl
chr19:11657898..11658000hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594678
Supporting Variants
SamplesHG03125
Known GenesCNN1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103810
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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