A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1638921



Internal ID12455355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40377402..40377402hg38UCSC Ensembl
chr19:40883309..40883309hg19UCSC Ensembl
chr19:45575149..45575149hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38104
hg19104
hg18104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4039232
SamplesHuRef
Known GenesPLD3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1638921
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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