A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763407



Internal ID18966300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45111205..45111426hg38UCSC Ensembl
chr11:45132756..45132977hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070447
Supporting Variants
SamplesKWP1
Known GenesPRDM11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763407
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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