A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052046



Internal ID19141265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18471488..18686425hg38UCSC Ensembl
Innerchr13:19045628..19260565hg19UCSC Ensembl
Innerchr13:17943628..18158565hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38214938
hg19214938
hg18214938
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1599n100
Supporting Variantsnssv3712696
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)nsv1052046
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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