A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385456



Internal ID21043009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87978552..87979361hg38UCSC Ensembl
chr4:88899704..88900513hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38810
hg19810
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214766
Samples
Known GenesSPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385456
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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