A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446160



Internal ID21103713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:2568057..2571672hg38UCSC Ensembl
chr10:2610249..2613864hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg383616
hg193616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979329
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446160
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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