A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153450



Internal ID21479557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105464667..105464759hg38UCSC Ensembl
chr8:106476895..106476987hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572216
Supporting Variants
SamplesHG03486
Known GenesZFPM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153450
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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