A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045198



Internal ID18787729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:46358308..46520002hg38UCSC Ensembl
Innerchr13:46932443..47094137hg19UCSC Ensembl
Innerchr13:45830444..45992138hg18UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg38161695
hg19161695
hg18161695
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3714981
Samples
Known GenesKIAA0226L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045198
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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