A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998582



Internal ID19158118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:68373537..68412040hg38UCSC Ensembl
Innerchr3:68422687..68461190hg19UCSC Ensembl
Innerchr3:68505377..68543880hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3838504
hg1938504
hg1838504
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593973
Samples
Known GenesFAM19A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998582
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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