A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039280



Internal ID19128499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:107469328..107549440hg38UCSC Ensembl
Innerchr13:108121676..108201788hg19UCSC Ensembl
Innerchr13:106919677..106999789hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3880113
hg1980113
hg1880113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1740n100
Supporting Variantsnssv3713301
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)nsv1039280
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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