A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069613



Internal ID19321485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86308281..86308460hg38UCSC Ensembl
chr11:86019323..86019502hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767203
SamplesKWP1
Known GenesC11orf73
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069613
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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