A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449121



Internal ID21106674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22332501..22355700hg38UCSC Ensembl
chr10:22621430..22644629hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3823200
hg1923200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194664
Samples
Known GenesSPAG6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449121
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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