A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3878358



Internal ID11883513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133111764..133111764hg38UCSC Ensembl
chr10:134925268..134925268hg19UCSC Ensembl
chr10:134775258..134775258hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38378
hg19378
hg18378
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1303257
Supporting Variants
SamplesHuRef
Known GenesGPR123
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3878358
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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