A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996963



Internal ID17289915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:120688823..120713822hg38UCSC Ensembl
Outerchr9:123451101..123476100hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3825000
hg1925000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950934
Supporting Variants
SamplesBILGI_BIOE
Known GenesMEGF9
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2996963
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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