A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151388



Internal ID19197139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:64367307..64372005hg38UCSC Ensembl
Outerchr9:43131099..43135800hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg384699
hg194702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003955
SamplesKWB1
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151388
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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