A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209270



Internal ID20776310
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 StatusS
Merged Variantsnsv6366717
Supporting Variants
Samples
Known GenesKIAA1143, KIF15, MIR564, TGM4, TMEM42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209270
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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