A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4349236



Internal ID11631774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83300566..83300851hg38UCSC Ensembl
chr4:84221719..84222004hg19UCSC Ensembl
chr4:84440743..84441028hg18UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38286
hg19286
hg18286
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1199239
Supporting Variants
SamplesHuRef
Known GenesHPSE
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4349236
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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