A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18166196



Internal ID20733236
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 StatusS
Merged Variantsnsv6426366
Supporting Variants
Samples
Known GenesKIF13B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18166196
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00076


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