A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479846



Internal ID21137399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:44580610..44662484hg38UCSC Ensembl
chr14:45049813..45131687hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3881875
hg1981875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018695
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479846
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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