A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1464086



Internal ID12280522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11402999..11403531hg38UCSC Ensembl
chr19:11513675..11514207hg19UCSC Ensembl
chr19:11374675..11375207hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38533
hg19533
hg18533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4036019
SamplesHuRef
Known GenesRGL3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1464086
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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