A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768519



Internal ID19315135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40219481..40223382hg38UCSC Ensembl
chr9:42364499..42368400hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg383902
hg193902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077111
Supporting Variants
SamplesKWP1
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768519
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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