A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362095



Internal ID21019648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25358020..25920032hg38UCSC Ensembl
chr4:25359642..25921654hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38562013
hg19562013
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211803
Samples
Known GenesANAPC4, SEL1L3, SLC34A2, SMIM20, ZCCHC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362095
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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