A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480160



Internal ID21137713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58096961..58136077hg38UCSC Ensembl
chr14:58563679..58602795hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3839117
hg1939117
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196281
Samples
Known GenesC14orf37
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480160
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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