A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389227



Internal ID21046780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:171799812..171808767hg38UCSC Ensembl
chr4:172720963..172729918hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg388956
hg198956
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214630
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389227
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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