A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365459



Internal ID21023012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6974994..6980755hg38UCSC Ensembl
chr4:6976721..6982482hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg385762
hg195762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119028
Samples
Known GenesTBC1D14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365459
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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