A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040965



Internal ID19130184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:66147517..66225131hg38UCSC Ensembl
Innerchr13:66721649..66799263hg19UCSC Ensembl
Innerchr13:65619650..65697264hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3877615
hg1977615
hg1877615
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3711835
Samples
Known GenesMIR4704
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040965
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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