A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211694



Internal ID20778734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6941292..6959040hg38UCSC Ensembl
chr4:6943019..6960767hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3817749
hg1917749
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374219
Supporting Variants
Samples
Known GenesTBC1D14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211694
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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