A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070462



Internal ID19320191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61508627..61508928hg38UCSC Ensembl
chr11:61276099..61276400hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763679
SamplesKWP1
Known GenesLRRC10B, MIR4488
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070462
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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