A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444606



Internal ID21102159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49231420..49269275hg38UCSC Ensembl
chr10:50439465..50477320hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3837856
hg1937856
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179560
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444606
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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