A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765188



Internal ID18962207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77019983..77020384hg38UCSC Ensembl
chr9:79634899..79635300hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075657
Supporting Variants
SamplesKWP1
Known GenesFOXB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765188
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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