A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4157141



Internal ID11439679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183414201..183414687hg38UCSC Ensembl
chr4:184335354..184335840hg19UCSC Ensembl
chr4:184572348..184572834hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38487
hg19487
hg18487
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1620699
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4157141
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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