A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385433



Internal ID21042986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:167024730..167028032hg38UCSC Ensembl
chr4:167945881..167949183hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg383303
hg193303
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213818
Samples
Known GenesSPOCK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385433
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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