A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451405



Internal ID21108958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:108367901..108376300hg38UCSC Ensembl
chr10:110127659..110136058hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg388400
hg198400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977397
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451405
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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