A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3649359



Internal ID12112509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183464268..183464334hg38UCSC Ensembl
chr4:184385421..184385487hg19UCSC Ensembl
chr4:184622415..184622481hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3867
hg1967
hg1867
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1262337
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3649359
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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