A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431408



Internal ID21088961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:104506800..104507218hg38UCSC Ensembl
chr8:105519028..105519446hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162731
Samples
Known GenesLRP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431408
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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