A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446157



Internal ID21103710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3666063..3681189hg38UCSC Ensembl
chr10:3708255..3723381hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg3815127
hg1915127
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186501
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446157
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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