A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438955



Internal ID21096508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79507301..79537800hg38UCSC Ensembl
chr10:81267057..81297556hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3830500
hg1930500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190049
Samples
Known GenesEIF5AL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438955
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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