A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211751



Internal ID20778791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16225001..16230700hg38UCSC Ensembl
chr4:16226624..16232323hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364809
Supporting Variants
Samples
Known GenesTAPT1, TAPT1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211751
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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