A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445982



Internal ID21103535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61452901..61454300hg38UCSC Ensembl
chr10:63212659..63214058hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190208
Samples
Known GenesTMEM26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445982
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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