A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450006



Internal ID21107559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44808301..44811600hg38UCSC Ensembl
chr10:45303749..45307048hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980373
Samples
Known GenesTMEM72-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450006
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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