A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005025



Internal ID18747556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:25563385..25575569hg38UCSC Ensembl
Innerchr3:25604876..25617060hg19UCSC Ensembl
Innerchr3:25579880..25592064hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3812185
hg1912185
hg1812185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4706n100
Supporting Variantsnssv3589511
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)nsv1005025
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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