A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766888



Internal ID18960976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132213741..132214051hg38UCSC Ensembl
chr11:132083635..132083945hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070996
Supporting Variants
SamplesKWP1
Known GenesNTM
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766888
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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