A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447792



Internal ID21105345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25046588..25104327hg38UCSC Ensembl
chr10:25335517..25393256hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3857740
hg1957740
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192220
Samples
Known GenesENKUR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447792
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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