A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046572



Internal ID19135791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:111027863..111099555hg38UCSC Ensembl
Innerchr13:111680210..111751902hg19UCSC Ensembl
Innerchr13:110478211..110549903hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3871693
hg1971693
hg1871693
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1742n100
Supporting Variantsnssv3713319, nssv3525602
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)nsv1046572
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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