A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892447



Internal ID19183267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113339931..113376029hg38UCSC Ensembl
Outerchr13:113339931..113376029hg38UCSC Ensembl
Innerchr13:113994246..114030344hg19UCSC Ensembl
Outerchr13:113994246..114030344hg19UCSC Ensembl
Innerchr13:113042247..113078345hg18UCSC Ensembl
Outerchr13:113042247..113078345hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3836099
hg1936099
hg1836099
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789633
Samples
Known GenesGRTP1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892447
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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