A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493711



Internal ID21151264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:26088258..26088635hg38UCSC Ensembl
chr14:26557464..26557841hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016849
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493711
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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