A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073794



Internal ID18972496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17408079..17408416hg38UCSC Ensembl
chr8:17265588..17265925hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770730
SamplesKWP1
Known GenesMTMR7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073794
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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