A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379856



Internal ID21037409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112219401..112238700hg38UCSC Ensembl
chr4:113140557..113159856hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3819300
hg1919300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5417n223
Supporting Variantsnssv18209543
Samples
Known GenesAP1AR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379856
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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