A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443909



Internal ID21101462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68300201..68304400hg38UCSC Ensembl
chr10:70059958..70064157hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983006
Samples
Known GenesPBLD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443909
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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