A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1086437



Internal ID11902875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70845663..70845663hg38UCSC Ensembl
chr10:72605420..72605420hg19UCSC Ensembl
chr10:72275426..72275426hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38319
hg19319
hg18319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4292985
SamplesHuRef
Known GenesSGPL1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1086437
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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