A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449281



Internal ID21106834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72943063..72949184hg38UCSC Ensembl
chr10:74702821..74708942hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg386122
hg196122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983838
Samples
Known GenesPLA2G12B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449281
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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