A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420586



Internal ID21078139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22183744..22186003hg38UCSC Ensembl
chr8:22041257..22043516hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg382260
hg192260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167074
Samples
Known GenesBMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420586
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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