A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454394



Internal ID21111947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91131587..91136284hg38UCSC Ensembl
chr10:92891344..92896041hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg384698
hg194698
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182839
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454394
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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