A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426366



Internal ID21083919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29126700..29127135hg38UCSC Ensembl
chr8:28984217..28984652hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166196
Samples
Known GenesKIF13B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426366
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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