A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011668



Internal ID19100885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65525221..65605743hg38UCSC Ensembl
Innerchr3:65510896..65591418hg19UCSC Ensembl
Innerchr3:65485936..65566458hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3880523
hg1980523
hg1880523
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593956
Samples
Known GenesMAGI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011668
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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