A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071316



Internal ID18970840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89648651..89648889hg38UCSC Ensembl
chr16:89715059..89715297hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765868
SamplesKWP1
Known GenesCHMP1A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071316
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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