A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115840



Internal ID18911700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:99004018..99006518hg38UCSC Ensembl
Outerchr9:101766300..101768800hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg382501
hg192501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977649
SamplesKWS2
Known GenesCOL15A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115840
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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