A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159592



Internal ID21427419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:107368450..107368849hg38UCSC Ensembl
chr8:108380678..108381077hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582612
Supporting Variants
SamplesHG00731
Known GenesANGPT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159592
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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