A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070369



Internal ID18970882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89647488..89648417hg38UCSC Ensembl
chr16:89713896..89714825hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38930
hg19930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771942
SamplesKWP1
Known GenesCHMP1A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070369
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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