A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765808



Internal ID18960139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6055406..6055907hg38UCSC Ensembl
chr10:6097369..6097870hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073083
Supporting Variants
SamplesKWP1
Known GenesIL2RA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765808
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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