A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069560



Internal ID18971817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9388321..9388374hg38UCSC Ensembl
chr11:9409868..9409921hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770150
SamplesKWP1
Known GenesIPO7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069560
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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