A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3573282



Internal ID6697979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6055418..6055915hg38UCSC Ensembl
chr10:6097381..6097878hg19UCSC Ensembl
chr10:6137387..6137884hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38498
hg19498
hg18498
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1011098
Supporting Variants
SamplesHuRef
Known GenesIL2RA
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3573282
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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