A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366717



Internal ID21024270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44759283..44881010hg38UCSC Ensembl
chr3:44800775..44922502hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38121728
hg19121728
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209270
Samples
Known GenesKIAA1143, KIF15, MIR564, TGM4, TMEM42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366717
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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