A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4136459



Internal ID11418998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96795907..96796636hg38UCSC Ensembl
chr10:98555664..98556393hg19UCSC Ensembl
chr10:98545654..98546383hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38730
hg19730
hg18730
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1640225
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4136459
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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