A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4189182



Internal ID11471720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15390866..15390960hg38UCSC Ensembl
chr3:15432373..15432467hg19UCSC Ensembl
chr3:15407377..15407471hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3895
hg1995
hg1895
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1505705
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4189182
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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