A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695217



Internal ID18993498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:120642332..120680372hg38UCSC Ensembl
Innerchr9:123404610..123442650hg19UCSC Ensembl
Innerchr9:122444431..122482471hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3838041
hg1938041
hg1838041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045180
Supporting Variants
Samples
Known GenesMEGF9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3695217
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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