A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766266



Internal ID18959701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122311304..122312205hg38UCSC Ensembl
chr5:121646999..121647900hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073492
Supporting Variants
SamplesKWP1
Known GenesSNCAIP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766266
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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