A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3711149



Internal ID12050721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74995000..74995480hg38UCSC Ensembl
chr14:75461703..75462183hg19UCSC Ensembl
chr14:74531456..74531936hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38481
hg19481
hg18481
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1124073
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3711149
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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