A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129003



Internal ID19262680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:64400923..64407214hg38UCSC Ensembl
Outerchr9:43095900..43102200hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg386292
hg196301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961675
SamplesKWS1
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129003
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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