A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444269



Internal ID21101822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47645001..47703700hg38UCSC Ensembl
chr10:49043987..49095536hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3858700
hg1951550
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv726n223
Supporting Variantsnssv18187771
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444269
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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