A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385179



Internal ID21042732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:175066338..175412140hg38UCSC Ensembl
chr4:175987489..176333291hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38345803
hg19345803
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212772
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385179
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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