A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766106



Internal ID19313870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32238680..32239081hg38UCSC Ensembl
chr17:30565699..30566100hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071379
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766106
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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