A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512129



Internal ID20885459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90825484..90825934hg38UCSC Ensembl
chr14:91291828..91292278hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183572
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512129
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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