A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393022



Internal ID21050575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:176318201..176320900hg38UCSC Ensembl
chr4:177239352..177242051hg19UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212782
Samples
Known GenesSPCS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393022
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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