A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070427



Internal ID18971266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2299969..2300470hg38UCSC Ensembl
chr11:2321199..2321700hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772167
SamplesKWP1
Known GenesC11orf21
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070427
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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