A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4100156



Internal ID11661719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67112335..67113266hg38UCSC Ensembl
chr15:67404673..67405604hg19UCSC Ensembl
chr15:65191727..65192658hg18UCSC Ensembl
Cytoband15q22.33
Allele length
AssemblyAllele length
hg38932
hg19932
hg18932
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1476959
Supporting Variants
SamplesHuRef
Known GenesSMAD3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4100156
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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