A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1057266



Internal ID11873705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15337639..15337639hg38UCSC Ensembl
chr10:15379638..15379638hg19UCSC Ensembl
chr10:15419644..15419644hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3853
hg1953
hg1853
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4089908
SamplesHuRef
Known GenesFAM171A1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1057266
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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