A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417048



Internal ID21074601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29114133..29119115hg38UCSC Ensembl
chr8:28971650..28976632hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg384983
hg194983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166194
Samples
Known GenesKIF13B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417048
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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