A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048206



Internal ID19137425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110943780..110999416hg38UCSC Ensembl
Innerchr13:111596127..111651763hg19UCSC Ensembl
Innerchr13:110394128..110449764hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3855637
hg1955637
hg1855637
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525585
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048206
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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