A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447053



Internal ID21104606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78967847..78970351hg38UCSC Ensembl
chr10:80727604..80730108hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382505
hg192505
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179554
Samples
Known GenesZMIZ1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447053
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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