A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444156



Internal ID21101709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25654319..25738978hg38UCSC Ensembl
chr10:25943248..26027907hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3884660
hg1984660
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193231
Samples
Known GenesLINC00836
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444156
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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