A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038111



Internal ID19127330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105755676..105832949hg38UCSC Ensembl
Innerchr13:106408025..106485298hg19UCSC Ensembl
Innerchr13:105206026..105283299hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3877274
hg1977274
hg1877274
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525569, nssv3713297, nssv3525568
Samples
Known GenesLINC00343
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038111
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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