A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146991



Internal ID19200938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:64384697..64391692hg38UCSC Ensembl
Outerchr9:43111399..43118400hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg386996
hg197002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998355
SamplesKWB1
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146991
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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