A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009124



Internal ID21918467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33644223..33672867hg38UCSC Ensembl
chr8:33501741..33530385hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3828645
hg1928645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569986
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009124
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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