A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005518



Internal ID19094735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151596556..151684342hg38UCSC Ensembl
Innerchr3:151314344..151402130hg19UCSC Ensembl
Innerchr3:152797034..152884820hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3887787
hg1987787
hg1887787
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606169
Samples
Known GenesMIR548H2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005518
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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