A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3803562



Internal ID11611623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2811856..2811856hg38UCSC Ensembl
chr19:2811854..2811854hg19UCSC Ensembl
chr19:2762854..2762854hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38215
hg19215
hg18215
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1039020
Supporting Variants
SamplesHuRef
Known GenesTHOP1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3803562
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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