A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484686



Internal ID21142239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23175941..23181058hg38UCSC Ensembl
chr14:23645150..23650267hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg385118
hg195118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016725
Samples
Known GenesSLC7A8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484686
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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