A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017638



Internal ID21926981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30736538..30736625hg38UCSC Ensembl
chr8:30594055..30594142hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557966
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017638
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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