A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3611350



Internal ID18909631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192214698..192230051hg38UCSC Ensembl
Innerchr3:191932487..191947840hg19UCSC Ensembl
Innerchr3:193415181..193430534hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3815354
hg1915354
hg1815354
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998673
Supporting Variants
Samples
Known GenesFGF12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3611350
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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