A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4149104



Internal ID11431642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177326883..177326936hg38UCSC Ensembl
chr5:176753884..176753937hg19UCSC Ensembl
chr5:176686490..176686543hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3854
hg1954
hg1854
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1603852
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4149104
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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