A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4338326



Internal ID11620864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118066583..118066812hg38UCSC Ensembl
chr4:118987738..118987967hg19UCSC Ensembl
chr4:119207186..119207415hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38230
hg19230
hg18230
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1771263
Supporting Variants
SamplesHuRef
Known GenesNDST3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4338326
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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