A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379921



Internal ID21037474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:98657901..98659700hg38UCSC Ensembl
chr4:99579052..99580851hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214403
Samples
Known GenesTSPAN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379921
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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