A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765611



Internal ID18967896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89907291..89909292hg38UCSC Ensembl
chr16:89973699..89975700hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg382002
hg192002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071318
Supporting Variants
SamplesKWP1
Known GenesTCF25
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765611
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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