A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996946



Internal ID17289898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:98164119..98169018hg38UCSC Ensembl
Outerchr9:100926401..100931300hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950915
Supporting Variants
SamplesBILGI_BIOE
Known GenesCORO2A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2996946
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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