A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505096



Internal ID20878362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91448957..91450285hg38UCSC Ensembl
chr14:91915301..91916629hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg381329
hg191329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022743
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505096
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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