A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381400



Internal ID21038953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:123380301..123462500hg38UCSC Ensembl
chr4:124301456..124383655hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg3882200
hg1982200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210243
Samples
Known GenesSPRY1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381400
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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