A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454807



Internal ID21112360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113439452..113787342hg38UCSC Ensembl
chr10:115199211..115547101hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38347891
hg19347891
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv889n223
Supporting Variantsnssv18183265
Samples
Known GenesCASP7, HABP2, MIR4483, NRAP, PLEKHS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454807
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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