A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3807791



Internal ID11607394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112398026..112398364hg38UCSC Ensembl
chr10:114157784..114158122hg19UCSC Ensembl
chr10:114147774..114148112hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38339
hg19339
hg18339
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1472658
Supporting Variants
SamplesHuRef
Known GenesACSL5
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3807791
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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