A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045417



Internal ID19134636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110951016..110989840hg38UCSC Ensembl
Innerchr13:111603363..111642187hg19UCSC Ensembl
Innerchr13:110401364..110440188hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3838825
hg1938825
hg1838825
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1741n100
Supporting Variantsnssv3525587, nssv3525586
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)nsv1045417
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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