A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488051



Internal ID21145604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:54427341..54427837hg38UCSC Ensembl
chr14:54894059..54894555hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg38497
hg19497
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020224
Samples
Known GenesCNIH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488051
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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