A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009977



Internal ID21919320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37788535..37788612hg38UCSC Ensembl
chr8:37646053..37646130hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563477
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009977
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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