A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008941



Internal ID19098159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:114715311..114744899hg38UCSC Ensembl
Innerchr3:114434158..114463746hg19UCSC Ensembl
Innerchr3:115916848..115946436hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3829589
hg1929589
hg1829589
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604467
Samples
Known GenesMIR4796, ZBTB20
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008941
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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