A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445431



Internal ID21102984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73491988..73493094hg38UCSC Ensembl
chr10:75251746..75252852hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381107
hg191107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983865
Samples
Known GenesPPP3CB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445431
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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