A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004065



Internal ID19093282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:25543343..25570244hg38UCSC Ensembl
Innerchr3:25584834..25611735hg19UCSC Ensembl
Innerchr3:25559838..25586739hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3826902
hg1926902
hg1826902
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4705n100
Supporting Variantsnssv3589509
Samples
Known GenesRARB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004065
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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