A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452617



Internal ID21110170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17378982..17386395hg38UCSC Ensembl
chr10:17420981..17428394hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg387414
hg197414
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192545
Samples
Known GenesST8SIA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452617
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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