A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038880



Internal ID19128099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:84058296..84287704hg38UCSC Ensembl
Innerchr13:84632431..84861839hg19UCSC Ensembl
Innerchr13:83530432..83759840hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38229409
hg19229409
hg18229409
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713253
Samples
Known GenesLINC00333, MIR548F1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038880
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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