A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069903



Internal ID18976209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2786798..2787599hg38UCSC Ensembl
chr16:2836799..2837600hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770434
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069903
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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