A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070931



Internal ID19316275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2885769..2888570hg38UCSC Ensembl
chr11:2906999..2909800hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382802
hg192802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766717
SamplesKWP1
Known GenesSLC22A18AS
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070931
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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