A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477659



Internal ID21135212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39695470..39696081hg38UCSC Ensembl
chr13:40269607..40270218hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008721
Samples
Known GenesCOG6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477659
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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