A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416382



Internal ID21073935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:12751313..12758212hg38UCSC Ensembl
chr8:12608822..12615721hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164996
Samples
Known GenesLONRF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416382
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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