A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140660



Internal ID21463610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11739420..11739756hg38UCSC Ensembl
chr8:11596929..11597265hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5583391
Supporting Variants
SamplesHG03009
Known GenesGATA4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140660
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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