A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038041



Internal ID19127260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:89498911..91319226hg38UCSC Ensembl
Innerchr13:90151165..91971480hg19UCSC Ensembl
Innerchr13:88949166..90769481hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg381820316
hg191820316
hg181820316
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713266
Samples
Known GenesLINC00353, LINC00379, LINC00380, LINC00410, LINC00559, MIR622
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038041
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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