A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043019



Internal ID18785550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95272331..95500362hg38UCSC Ensembl
Innerchr13:95924585..96152616hg19UCSC Ensembl
Innerchr13:94722586..94950617hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38228032
hg19228032
hg18228032
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525496
Samples
Known GenesABCC4, CLDN10, CLDN10-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043019
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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