A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448862



Internal ID21106415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131046965..131050401hg38UCSC Ensembl
chr10:132845228..132848664hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg383437
hg193437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980696
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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