A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071314



Internal ID18973951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89489791..89490592hg38UCSC Ensembl
chr16:89556199..89557000hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765712
SamplesKWP1
Known GenesANKRD11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071314
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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