A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103037



Internal ID21463036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10547725..10548058hg38UCSC Ensembl
chr19:10658401..10658734hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590135
Supporting Variants
SamplesHG03009
Known GenesATG4D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103037
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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