A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3949144



Internal ID11466042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6055423..6055921hg38UCSC Ensembl
chr10:6097386..6097884hg19UCSC Ensembl
chr10:6137392..6137890hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38499
hg19499
hg18499
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1592945
Supporting Variants
SamplesHuRef
Known GenesIL2RA
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3949144
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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