A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455216



Internal ID21112769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24999101..25001100hg38UCSC Ensembl
chr10:25288030..25290029hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979279
Samples
Known GenesENKUR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455216
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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