A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766533



Internal ID18965867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:169079294..169079895hg38UCSC Ensembl
chr5:168506299..168506900hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074886
Supporting Variants
SamplesKWP1
Known GenesSLIT3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766533
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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