A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000748



Internal ID21910091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101671824..101671968hg38UCSC Ensembl
chr8:102684052..102684196hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592015
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000748
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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