A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014334



Internal ID21923677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61033313..61033462hg38UCSC Ensembl
chr8:61945872..61946021hg19UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014334
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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