A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489795



Internal ID21147348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51911625..51912184hg38UCSC Ensembl
chr14:52378343..52378902hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019157
Samples
Known GenesGNG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489795
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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