A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431436



Internal ID21088989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25854066..25854826hg38UCSC Ensembl
chr8:25711582..25712342hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38761
hg19761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167917
Samples
Known GenesEBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431436
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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