A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3423936



Internal ID15270893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107822044..107822063hg38UCSC Ensembl
Innerchr13:107822040..107822067hg38UCSC Ensembl
Outerchr13:107822021..107822086hg38UCSC Ensembl
chr13:108474392..108474411hg19UCSC Ensembl
Innerchr13:108474388..108474415hg19UCSC Ensembl
Outerchr13:108474369..108474434hg19UCSC Ensembl
chr13:107272393..107272412hg18UCSC Ensembl
Innerchr13:107272416..107272389hg18UCSC Ensembl
Outerchr13:107272370..107272435hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8677933
SamplesNA19240
Known GenesFAM155A
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3423936
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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