A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452280



Internal ID21109833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43835254..43838749hg38UCSC Ensembl
chr10:44330702..44334197hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg383496
hg193496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980302
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452280
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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