A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077841



Internal ID18978838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36166319..36168842hg38UCSC Ensembl
chr17:34493699..34496200hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg382524
hg192502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762802
SamplesKWP1
Known GenesTBC1D3B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077841
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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