A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071374



Internal ID19326470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18213291..18213349hg38UCSC Ensembl
chr17:18116605..18116663hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768606
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071374
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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