A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037686



Internal ID18780217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:110338326..110393343hg38UCSC Ensembl
Innerchr9:113100606..113155623hg19UCSC Ensembl
Innerchr9:112140427..112195444hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3855018
hg1955018
hg1855018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695047
Samples
Known GenesSVEP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037686
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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