A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3845434



Internal ID11569751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1148720..1148979hg38UCSC Ensembl
chr19:1148719..1148978hg19UCSC Ensembl
chr19:1099719..1099978hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38260
hg19260
hg18260
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1785958
Supporting Variants
SamplesHuRef
Known GenesSBNO2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3845434
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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