A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1195185



Internal ID12011622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14568390..14568390hg38UCSC Ensembl
chr10:14610389..14610389hg19UCSC Ensembl
chr10:14650395..14650395hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38206
hg19206
hg18206
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3727183
SamplesHuRef
Known GenesFAM107B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1195185
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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