A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892396



Internal ID19183216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:78300788..78333291hg38UCSC Ensembl
Outerchr13:78295146..78360426hg38UCSC Ensembl
Innerchr13:78874923..78907426hg19UCSC Ensembl
Outerchr13:78869281..78934561hg19UCSC Ensembl
Innerchr13:77772924..77805427hg18UCSC Ensembl
Outerchr13:77767282..77832562hg18UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3865281
hg1965281
hg1865281
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789076, essv25790128, essv25789219, essv25789485, essv25789086
Samples
Known GenesRNF219-AS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892396
Frequency
Sample Size3017
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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