A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069570



Internal ID19318834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31372223..31376108hg38UCSC Ensembl
chr11:31393770..31397655hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383886
hg193886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768316
SamplesKWP1
Known GenesDNAJC24
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069570
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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