A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003732



Internal ID19092950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:186888059..186967511hg38UCSC Ensembl
Innerchr3:186605848..186685299hg19UCSC Ensembl
Innerchr3:188088542..188167993hg18UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3879453
hg1979452
hg1879452
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3615037
Samples
Known GenesST6GAL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003732
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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