A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1495928



Internal ID12659050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5761619..5761619hg38UCSC Ensembl
chr19:5761630..5761630hg19UCSC Ensembl
chr19:5712630..5712630hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38155
hg19155
hg18155
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4264021
SamplesHuRef
Known GenesCATSPERD
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1495928
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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