A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1348586



Internal ID5478690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49622040..49622040hg38UCSC Ensembl
chr10:50830086..50830086hg19UCSC Ensembl
chr10:50500092..50500092hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38132
hg19132
hg18132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4059620
SamplesHuRef
Known GenesCHAT
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1348586
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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