A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050833



Internal ID18793364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:107200567..107404351hg38UCSC Ensembl
Innerchr13:107852915..108056699hg19UCSC Ensembl
Innerchr13:106650916..106854700hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38203785
hg19203785
hg18203785
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713300
Samples
Known GenesFAM155A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050833
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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