A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418960



Internal ID21076513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47567379..47592980hg38UCSC Ensembl
chr8:48479941..48505542hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3825602
hg1925602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167690
Samples
Known GenesSPIDR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418960
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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