A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046560



Internal ID19135779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:47251888..47280290hg38UCSC Ensembl
Innerchr13:47826023..47854425hg19UCSC Ensembl
Innerchr13:46724024..46752426hg18UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3828403
hg1928403
hg1828403
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523429
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)nsv1046560
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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