A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011784



Internal ID19101002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:95961320..96000822hg38UCSC Ensembl
Innerchr3:95680164..95719666hg19UCSC Ensembl
Innerchr3:97162854..97202356hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3839503
hg1939503
hg1839503
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4816n100
Supporting Variantsnssv3603304
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011784
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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