A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492989



Internal ID21150542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22629585..22644003hg38UCSC Ensembl
chr14:23098490..23113212hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3814419
hg1914723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016087
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492989
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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