A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765068



Internal ID18959530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69189570..69190074hg38UCSC Ensembl
chr9:71804486..71804990hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38505
hg19505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075246
Supporting Variants
SamplesKWP1
Known GenesTJP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765068
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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