A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998567



Internal ID16944833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:106860256..106867455hg38UCSC Ensembl
Outerchr7:106500701..106507900hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv949926
Supporting Variants
SamplesBILGI_BIOE
Known GenesPIK3CG
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998567
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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