A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3965064



Internal ID11450122
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1638639
Supporting Variants
SamplesHuRef
Known GenesSLIT1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3965064
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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