A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484962



Internal ID21142515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27338288..27418494hg38UCSC Ensembl
chr14:27807494..27887700hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3880207
hg1980207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2082n223
Supporting Variantsnssv18016670
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484962
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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