A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447690



Internal ID21105243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119872001..119875100hg38UCSC Ensembl
chr10:121631513..121634612hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186777
Samples
Known GenesMCMBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447690
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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