A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209486



Internal ID20776526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106251301..106265000hg38UCSC Ensembl
chr4:107172458..107186157hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3813700
hg1913700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6393971
Supporting Variants
Samples
Known GenesTBCK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209486
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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