A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070495



Internal ID18976598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128692204..128692805hg38UCSC Ensembl
chr11:128562099..128562700hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770967
SamplesKWP1
Known GenesFLI1, SENCR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070495
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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