A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713301



Internal ID19011582
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 StatusS
Merged Variantsnsv1039280
Supporting Variants
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)nssv3713301
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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