A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768289



Internal ID19311360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109320319..109320820hg38UCSC Ensembl
chr9:112082599..112083100hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077171
Supporting Variants
SamplesKWP1
Known GenesEPB41L4B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768289
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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