A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1638639



Internal ID12455072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97141681..97141736hg38UCSC Ensembl
chr10:98901438..98901493hg19UCSC Ensembl
chr10:98891428..98891483hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3856
hg1956
hg1856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3965064
SamplesHuRef
Known GenesSLIT1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1638639
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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