A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050836



Internal ID19140055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70577235..70670775hg38UCSC Ensembl
Innerchr13:71151367..71244907hg19UCSC Ensembl
Innerchr13:70049368..70142908hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3893541
hg1993541
hg1893541
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713239
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)nsv1050836
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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