A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485582



Internal ID21143135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25028474..25029994hg38UCSC Ensembl
chr14:25497680..25499200hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg381521
hg191521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016261
Samples
Known GenesSTXBP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485582
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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