A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497976



Internal ID20871184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103824131..103878033hg38UCSC Ensembl
chr14:104290468..104344370hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3853903
hg1953903
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189918
Samples
Known GenesLINC00637, PPP1R13B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497976
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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