A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499746



Internal ID20872969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92203583..92473100hg38UCSC Ensembl
chr14:92669927..92939444hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38269518
hg19269518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021812
Samples
Known GenesSLC24A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499746
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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