A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4159997



Internal ID11442535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186803104..186803943hg38UCSC Ensembl
chr3:186520893..186521732hg19UCSC Ensembl
chr3:188003587..188004426hg18UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38840
hg19840
hg18840
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1293846
Supporting Variants
SamplesHuRef
Known GenesRFC4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4159997
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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