A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738791



Internal ID20514762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:751036..751115hg38UCSC Ensembl
chr8:701036..701115hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263192
Samples
Known GenesERICH1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738791
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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