A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3793930



Internal ID11621255
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1158347
Supporting Variants
SamplesHuRef
Known GenesMTA1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3793930
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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