A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378783



Internal ID21036336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:176319301..176321600hg38UCSC Ensembl
chr4:177240452..177242751hg19UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212783
Samples
Known GenesSPCS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378783
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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