A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438205



Internal ID21095758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34860324..35275640hg38UCSC Ensembl
chr10:35149252..35564568hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38415317
hg19415317
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv685n223
Supporting Variantsnssv18194360
Samples
Known GenesCCNY, CREM, CUL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438205
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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