A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436461



Internal ID21094014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25157582..25158009hg38UCSC Ensembl
chr10:25446511..25446938hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979284
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436461
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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