A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492727



Internal ID21150280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21443193..21470997hg38UCSC Ensembl
chr14:21911352..21939156hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3827805
hg1927805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016017
Samples
Known GenesRAB2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492727
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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