A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv352n106



Internal ID20159709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6055407..6055920hg38UCSC Ensembl
chr10:6097370..6097883hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1130286, nsv1129886, nsv1127396
SamplesKWS1, KWS2
Known GenesIL2RA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv352n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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