A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479583



Internal ID21137136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:40599312..40824881hg38UCSC Ensembl
chr14:41068517..41294086hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38225570
hg19225570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2111n223
Supporting Variantsnssv18017490
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479583
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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