A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192675



Internal ID20759715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90680401..90685700hg38UCSC Ensembl
chr14:91146745..91152044hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504404
Supporting Variants
Samples
Known GenesTTC7B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192675
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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