A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115803



Internal ID19284674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:40236482..40244882hg38UCSC Ensembl
Outerchr9:42381500..42389900hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg388401
hg198401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977612
SamplesKWS2
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115803
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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