A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014890



Internal ID18757425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192694306..192885274hg38UCSC Ensembl
Innerchr3:192412095..192603063hg19UCSC Ensembl
Innerchr3:193894789..194085757hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38190969
hg19190969
hg18190969
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5010n100
Supporting Variantsnssv3611354
Samples
Known GenesFGF12, MB21D2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014890
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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