A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1542493



Internal ID12705614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41361796..41362088hg38UCSC Ensembl
chr19:41867701..41867993hg19UCSC Ensembl
chr19:46559541..46559833hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38293
hg19293
hg18293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3921631
SamplesHuRef
Known GenesB9D2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1542493
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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