A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3704076



Internal ID11711108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2805909..2805965hg38UCSC Ensembl
chr19:2805907..2805963hg19UCSC Ensembl
chr19:2756907..2756963hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3857
hg1957
hg1857
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1432748
Supporting Variants
SamplesHuRef
Known GenesTHOP1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3704076
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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