A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1158347



Internal ID11974784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105459221..105459752hg38UCSC Ensembl
chr14:105925558..105926089hg19UCSC Ensembl
chr14:104996603..104997134hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38532
hg19532
hg18532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3793930
SamplesHuRef
Known GenesMTA1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1158347
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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