A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4013454



Internal ID22075085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:10814955..10930030hg38UCSC Ensembl
Outerchr19:10802678..10940323hg38UCSC Ensembl
Innerchr19:10925631..11040706hg19UCSC Ensembl
Outerchr19:10913354..11050999hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38137646
hg19137646
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155553
Supporting Variants
Samples
Known GenesC19orf38, C19orf52, CARM1, DNM2, MIR199A1, MIR6793, TMED1, YIPF2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4013454
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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