A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425600



Internal ID21083153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119086264..119086949hg38UCSC Ensembl
chr8:120098503..120099188hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164136
Samples
Known GenesCOLEC10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425600
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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