A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008057



Internal ID18750588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:93800622..93905312hg38UCSC Ensembl
Innerchr3:93519466..93624156hg19UCSC Ensembl
Innerchr3:95002156..95106846hg18UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg38104691
hg19104691
hg18104691
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3603298
Samples
Known GenesPROS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008057
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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