A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3599644



Internal ID11815538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:105088512..105088579hg38UCSC Ensembl
chr10:106848270..106848337hg19UCSC Ensembl
chr10:106838260..106838327hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3868
hg1968
hg1868
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1433381
Supporting Variants
SamplesHuRef
Known GenesSORCS3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3599644
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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