A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736162



Internal ID20512108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35089856..35089932hg38UCSC Ensembl
chr8:34947374..34947450hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267368
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736162
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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